ORGANOPHOSPHORUS AMINES USED AS PLANT GROWTH REGULANTS

COMMONWEALTH OP AUSTRALIA PATENTS ACT 1952 Application Number: Lodged: Complete specification: Lodged: Accepted: Published: Priority: Related Art: FORM CASE: 09-21(2660)A AS Class: Int. Class Name of Applicant: MONSANTO COMPANY Address of Applicant: 800 North Lindbergh Boulevard, St, Louis, Missouri 63177, U.SiA, Actual Inventor: DONALD LEE FIELDS, JR.; cind RAYMOND CHARLES GRABIAK. Address for Service: E.F. WELLINGTON & CO., Patent and Trade Mark Attorneys, 457 St. Kilda Road, Melbourne, 3004, Victoria. Complete Specification for the invention entitled; "AMINE SALTS OF l,4,2-OXAZAPHOSPHOLIDINE-4-ACETIC ACID,, 2-ALKOXY-2-OXIDES,, The following statement is a full description of this invention including the best method of performing it known to us. :4 i .1 - 09-21(2660)A flit! C t I Background of the Invention This invention relates to novel organophos- phorus amines, and more particularly relates to novel amine salts of l,4,2-oxazaphospholidine-4-acetic acid, 2-alkoxy-2-oxides and the use of such compounds as a herbicide and plant growth regulator. There are numerous references in the prior art that disclose various organophosphorus compounds. For example, U.S. Patent 3,172,903 discloses that cer- tain 1,3,2-oxazaphospholidine and 1,3,2-oxazaphospho- lidine phosphorus ester compounds are useful as fungi¬ cides. U.S. Patent 4,190,651 discloses that certain 4-substituted 1,3,2-oxazaphospholidine derivatives discloses a synergistic insecticidial composition con¬ taining 2-(thi)oxo-l,3,2-oxazaphospholane of defined formula. Other organophosphorus compounds are known to have biological activity on plants. For example, U.S. Patent 3,799,758 to Franz discloses that N-phos- phonomethj-lglycine and its salts are useful as a broad spectrum herbicide and has a phytotoxic effect on most terrestrial and aquatic plants. U.S. Patent 4,486,359 to Brendel et al discloses that N-phosphondmethyl- glycine can be prepared from glycine and paraformal¬ dehyde to obtain an intermediate which is reacted with a dialkylphosphite to obtain an ester of the desired compound, which is then hydrolized. U.S. Patent 4,062,669 to Franz disloses that N-organo-N-phosphono- methylglycine-N-oxides and derivatives thereof are useful in herbicidal compositions and methods, and that the compounds and the compositions containing them are useful as phytotoxicants and as plant growth •MHM** 09-21(2660)A •fc" regulants. U.S. Patent 4,601,744 to Sikorski et al discloses that esters of NjN'-methylene-bis-tN-C- (diaryloxyphosphinyl)methyl]glycine] are useful as herbicides. Despite these and other references in the prior art, there is now provided a novel 1,4,2- oxazaphospholidine compounds that have selective phytotoxic activity, i.e. they have a herbicidal ef¬ fect upon certain plant species but do not have a phytotoxic effect on other plant species, and have a plant growth regulant activity, i.e. stunt or retard the growth rate of certain plants without phytotoxic- ity. Summary of the Invention These and other advantages are achieved by compounds represented by the formula: O i • * H2C - C - OH I N / V £12 C CH2 1 i I OR* wherein R4 is an alkyl group halving from 1 to about 4 carbon atoms. A particularly preferred embodiment of this invention is the tertiary amine salt of the 1,4,2-oxazaphospholidine-4-aGetie acid, 2-alkoxy-2- oxide represented by the above formula, and which amine salt can be represented by the following structural formula: ~r' *-,iW,*tf9W**><f*«*«WTOSSiti wsiwinasfflwawffljBitij jKa, ,3- 09-21(2660)A f ft t » HgC - C - OH • N-R1I i 1N/ \H2 C CHg1 1 1R3 1 1o=p—01 1OR4 wherein R1, R2 and R3 are individually selected from alkyl groups having from one to about four carbon atoms, Detailed Description of the Invention Although applicants do not wish to be bound by any particular theory, it is believied that the l,4,2-oxazaphospholidine-4-acetic acid, 2-alkoxy-2- oxide compounds of the present invention, represented by the above formulas, enter the plant and form an anidn as represented by the following structural formula: H2C - C - 0 I N H,2 C CHg I 1 0=P—o I OR4 wherein R4 is as defined above* It is believed that this anion is responsible for the selective herbici- dal activity and plant growth regulant properties ex¬ hibited by the novel compounds of the present inven¬ tion. The compounds of the presertt invention can be prepared from the known reaetants, glycihe, formal- dehyde, trialkylamine and dialkyl phosphite, i.e. dimethyl phosphite, diethyl phosphite, methylethyl- phosphite, diisopropylphosphite, dibutylphosphite and iiiulM—fr ' 09-21(2660)A * c f t * t t t r t c t t t C t t f I ft r « t ft t * t * t * c t r t the like. Mixed esters and branched derivatives can also be used. DimethyIphosphite and diethylphosphite are preferred. Another reactant is a trialkyl amine where- in the alkyl group contains from one to about four carbon atoms. Examples of such trialkyl amines include trimethylamine, triethylamine, tributylamine, triisopropylamine, tri-t-butylamine, and mixtures such as diethyImethy1amine, dibutylethylamine, and the like. Trimethylamine and triethylamine are preferred, since they are readily available. To prepare the compounds of the present in¬ vention, formaldehyde and a trialkylamine are heated to solution in an anhydrous solvent, such as methanol, IS ethanol, propanol, isopropynol, t-bitynol, butanol, and the like. Methanol is preferred. Thereafter, -glycine is added with heat and stirring, and then the dialkyl phosphite is added to the solution and heated. There is then provided the trialkylamine salt of l,4,2-oxazaphospholidine-4-acetic acid, 2-alkoxy-2- oxide. The acid can be prepared by passing the solution of the amine salt in anhydrous alcohol through a weakly acidic cation exchange resin to remove the trialkylamine and provide the 1,4,2-oxa- zaphospholidine-4-acetic acid, 2-aikoxy-2-oxides. The mdle ratio of the reactants influences the yield of the desired product. In general, most of the reactants are in a mole ratio of about 1:1, based on glycine, except that foirmaldehyde should be used in excess, preferably 2:1 or 3:1 or higher. The temperature of the dialkyl phosphite addition can vary from about room temperature to about 75°C. Satisfactory results have been achieved at 3S temperatures between about 250C and about 60bC. v t 'fes? ii i <t0a$i -5- 0921(2660)A The products of the above reaction are use¬ ful as selective post emergent herbicides by providing phytotoxic activity on cocklebur, morningglory, barnyardgrass, yellow nutsedge and quackgrass. The compounds are also useful to control the growth rate on desirable grasses, such as fescue. Typically the biologically active compounds of this invention are provided in the form of concen¬ trates which require dilution prior to application to plants. The usual means for diluting the concentrate, whether either liquid or solid, comprising adjuvants, inert materials and the like, are known to those skilled in the art. The compositions containing concentrates which require dilution prior to applica- tion to the plants contain from about 5 to 95 parts by weight of at least one compound of the present invention, and from 5 to 95 parts by weight of an adjuvant in liquid or solid form, for example, from about 0.25 to 25 parts by weight of a wetting agent, from about 0.25 to 25 parts by weight of a dispersant, and from about 4.5 to about 94.5 parts by weight of an inert liquid extender, such as water, acetone, tetra- hydrofuran and the like. The composition can also contain other materials as will occur to those skilled in the art in view of this disclosure. When operating in accordance with the teachings of the present invention, effective amounts of the compounds or compositions of the present inven¬ tion are applied to the plants or are incorporated into aquatic media in any conventional fashion. The compositions can also be applied from airplanes as a dust or spray by means known to those skilled in the art. The application of an effective amount of the compound or composition of the present invention »™*~-i*-™>«'Mj«i((li»»$«i«es mwwwi * • H t • 4 « ft t I t t « -6- 09-21(2660)A to the plant is essential and critical for the prac¬ tice of the present invention. The exact amount of the active ingredient to be employed is dependent upon the response desired in the plant, as well as such other factors such as the plant species, stage of development, the amount of rainfall, as well as the specific compound employed. It is believed that one skilled in the art can readily determine from the teachings of this specification, including the examples, the approximate application rate. The invention is further illustrated by, but not limited to, the following examples, where all per¬ centages are by weight unless otherwise indicated. Example 1 Preparation of triethylamine salt of 1,4,2- oxazaphos- pholidine-4-acetic acid, 2-methoxy-2-oxide. Triethylamine (5.05 g, 0.05 mol) and para¬ formaldehyde (3.0 g, 0.10 mol) were heated to solution (550C) in methanol (50 ml). Glycine (3.75 g, G.05 mol) was added in one portion and the mixture was heated at reflux for one hour. The solution was cooled to room temperature, and dimethyl phosphite (5.5 g, 0.05 mol) was added in one portion. The solution was heated at reflux for 40 minutes upon which time the 31P NMR spectra showed the absence of dimethyl phosphite. The methanol in the reaction mixture was removed on a rotary evaporator at 350C and reduced pressure (25 mm, SS.SSxlON/m2) to yield 15.4 g of a light yellow oil, which was confirmed to be the desired compound by 1H NMR, 13C NMR an$ 31P NMR spectral analyses. Example 2 Preparation of l,4,2-Qxazaphospholidine-4- acetic acid, 2-alkoxy-2-oxide< The procedure of Example 1 was repeated to obtain the light yellow oil, which was then dissolved 09-21(2660)A in methanol (50 ml) and the solution was passed through a 30 cm long column of Amberlite™ CG-50 slightly acetic cation exchange resin available from Rohm & Haas Company of West Philadelphia, Pennsylvania. Analysis by 1H NMR, 13C NMR and 31P NMR confirmed the presence of the desired compound. Example 3 Post-Emergent Herbicide Activity. The post-emergent herbicidal activity of the compound of Example 1 was demonstrated by greenhouse testing. Top soil was placed in pans having holes in the bottom and compacted to a depth of 0.95 to 1.27 cm from the top of the pan. A predetermined number of seeds of each of several plant species or vegetative propagules for perennial plant species were placed on the soil and pressed into the soil surface. The seeds or propagules were covered with soil and leveled. The pans were then placed on a bench in the greenhouse and watered as needed for germination and growth. After the plants reached the desired age (2 to 3 weeks) each pan? except the control pans, was removed to a spray¬ ing chamber and sprayed by means of an atomizer* In the spray solution, an emulsifying agent was added to give a spray solution which contains about 0.4% by volume of the emulsifier. The spray solution con¬ tained a sufficient amount of the compound of Example 1 to give an application rate of the active ingredient of 2.8 g/m2 (25 lbs. per acre) and 5.6 g/m2 (50 lbs. per acre), while applying a total Amount of solution equivalent to 187 ml/m2 (200 gal per acre). The pans were returned to the greenhouse and watered as before, and the injury to the plants as compared to those in control pans was observed after 14 days after spray¬ ing, and again, 27 days after spraying. After 27 days the post emergent herbicide JiiSKiigMHeMigaiysewa wnmMiiimmummiftf «a e 09-21(2660)A activity was observed at a rate of application of 5.6 g/m2. The data are shown in Table I. Table I Plant Plant Response* AfterSpecies 14 Days 27 Days Canada Thistle 0 0 Cocklebur 1 1 Velvetleaf 0 0 Morningglory 1 1 Common Lambsquarters 0 0 Pennsylvania smartweed 0 0 Yellow Nutsedge 0 1 Quackgrass 0 1 Rhizone Johnsongrass 0 0 Downy Brome 0 0 Barnyardgrass 1 1 *Plant Response Index 0 - 24% inhibition 0 - 49% inhibition 1 - 74% inhibition 2 75 - 99% inhibition 3 100% inhibition 4 Example 4 Plant Growth Regulating Activity. The plant growth regulating activity of the compound of Example 1 was demonstrated by greenhouse testing. Established stands of fescue (Kentucky bluegrass No. 31) in pots having an area of about 100 dm (16 square inches) were triihmed to a uniform height. Duplicate pots Were removed to a spraying chamber and sprayed by means of an atomizer as in -9. 09-21(2660)A Example 3. The application rate of the active ingre¬ dient was 0,56 g/m2 (5 lbs. per acre) while applying a total amount of solution equivalent to 187 ml/m2 (200 gal/acre). The pots were returned to the greenhouse and watered with the controls on a daily basis. After two weeks, the height of the grass was measured. The control pots grew ah average of 199.58 mm over the two-week period, and the pots treated with the compound of Example 1 grew 80 and 90 mm, showing that the treated fescue had an average growth rate of 43% of the controls. The grass did not show any discoloration or other sign of phytotoxicity. Example Preparation of Triisopropylamine Salt of 1,4,2-Oxaza- phospholidine-4-Acetic Acid, 2-Methoxy-2-Oxide. The procedure of Example 1 is repeated except that 0.05 mol of triisopropylamine is substi¬ tuted for the triethylamine used in Example 1. Analysis by spectral data indicates the presence of the desired triisopropylamine salt of 1,4,2-oxazaphos- pholidine-4-acetic acid, 2-methoxy-2-oxide. Example 6 Biological Activity, The compound of Example 2 and the compound of Example 5 is tested in greenhouse tests according to the procedure of Examples 3 and 4. Satisfactory results are achieved. Although the invention has been described in terms of specified embodiments, which are set forth in considerable detail, it should be understood that this is by way of illustration only, and that altern¬ ative embodiments and operating techniques will be¬ come apparent to those skilled in the art in view of wii-****-** *&&*w*&*i!H&fi&r>t 4!togg8ii0g!Qsii&<m#H!&mm>e3>*& r/ZS*IWltJlHJ%*9*rssHiJM*m*-m*e**-* if 09-21(2660)A the disclosure. For example, other salts of the l,4f2-Qxazaphospholidine-4-acetic acid, 2-alkoxy-2- oxide of the present invention, such as the sulfate, chloride, bromide, and the like can be substituted for the trialkylamine, provided they do not cause decompo¬ sition of the acid- Accordingly, modifications can be made without departing from the spirit of the desribed invention as defined in the following claims. The matter contained in each of the following claims is to be read as part of the general description of the present invention. i * • • • i i l f a ( WSffiWsSWiJiKWfiWsy % ** 1 I V « « s * t # 4 r i e X C I 4 * » 4 1 F » a t r t t i * I K -U- 09-21(2660)A The claims defining the invention are as follows: 1. A compound represented by the formula: II H2C - C - OH I N H2 C CH2 I I 0=1—o I OR4 wherein R4 is an alkyl having from one to about four carbon atoms. 2. A compound of Claim 1 wherein R4 is methyl. 3. A compound of Claim 1 wherein R4 is ethyl. 4. A compound of Claim 1 as the trialkyl- amine salt which is represented by the formula: O R2 II I H2C - C - OH • N - R1 I I N R3 H2 C CH2 I I 0=p—o I OR4 wherein R1, R2 and R3 are individually selected from the group consisting of alkyl having from One to about four carbon atoms. 5. A compound of Claim 4 wherein &, R2, R3 and R4 are independently selected from methyl or ethyl * 6. A compound ef Claim 4 wherein R1, R2 and R3 are ethyl and R is methyl.