US4565782A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Process for producing optically active aryloxypropionic acids and derivatives thereof useful as herbicides
Assignee: Imperial Chemical Industries Ltd
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Filing: 1984-07-26
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Granted: 1986-01-21
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Expires: 2004-07-26
Abstract
Abstract A process for the stereospecific inversion of the [S] enantiomer of an alpha -aryloxypropionic acid of formula I: <IMAGE> (I) wherein E is OR1 or <IMAGE> R1 is an unsubstituted or substituted aryl or heterocyclic ring system, and R2 is hydrogen or methyl, U and V each independently represent hydrogen or halogen and R is a carboxyl group, or an enzymic and herbicidal equivalent thereof, which process comprises contacting said [S] enantiomer with a microorganism having a stereospecific inverting enzyme system, or with an extract of the microorganism containing said enzyme system, to convert the [S] enantiomer to the corresponding [R] enantiomer.
Inventors
- 👤 David W. Bewick
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 17:28
CPC Classifications
C; C07; C07D; C07D213/00; C07D213/02; C07D213/04; C07D213/60; C07D213/62; C07D213/63; C07D213/64; C07D213/643; C07D241/00; C07D241/36; C07D241/38; C07D241/40; C07D241/44; C07D277/00; C07D277/60; C07D277/62; C07D277/68; C12; C12P; C12P13/00; C12P13/001; C12P17/00; C12P17/10; C12P17/12; C12P17/16; C12P17/18; C12P41/00; C12P7/00; C12P7/40; Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/55
Claims Analysis
Total Claims: 14
Claim 1
Independent Claim
105 words
A process for the stereospecific inversion of the enantiomer of an α-aryloxypropionic acid of formula I: ##STR15## wherein E is OR 1 or ##STR16## R 1 is an unsubstituted or substituted aryl or heterocyclic ring system, and R 2 is hydrogen or methyl, U and V each independently represent hydrogen or halogen and R is a carboxyl group, or an enzymic and herbicidal equivalent thereof, in a mixture with its [R] enantiomer, which process comprises contacting said [S] enantiomer with a stereospecific inverting enzyme so as to convert the [S] enantiomer to the corresponding [R] enantiomer without substantially affecting the [R] enantiomer in said mixture.
Claim 2
Dependent Claim
105 words
A process for the stereospecific inversion of the enantiomer of an α-aryloxypropionic acid of formula I: ##STR15## wherein E is OR 1 or ##STR16## R 1 is an unsubstituted or substituted aryl or heterocyclic ring system, and R 2 is hydrogen or methyl, U and V each independently represent hydrogen or halogen and R is a carboxyl group, or an enzymic and herbicidal equivalent thereof, in a mixture with its [R] enantiomer, which process comprises contacting said [S] enantiomer with a stereospecific inverting enzyme so as to convert the [S] enantiomer to the corresponding [R] enantiomer without substantially affecting the [R] enantiomer in said mixture.
Claim 3
Dependent Claim
12 words
A process according to claim 1 wherein the enzyme comprises a bacterium.
Claim 4
Dependent Claim
15 words
A process according to claim 2 wherein the bacterium is chosen from the Actinomycetales organisms.
Claim 5
Dependent Claim
12 words
A process according to claim 3 wherein the bacterium is a Rhodococcus.
Claim 6
Dependent Claim
29 words
A process according to claim 1 wherein the enzyme comprises: a Rhodococcus sp. (NCIB 11880), Rhodococcus rhodochrous (ATCC 13808), a Rhodococcus sp. (NCIB 11276), or Botrytis cinerea (ATCC 28387).
Claim 7
Dependent Claim
75 words
A process according to claim 1 wherein the enzyme comprises: Arthrobacter simplex (NCIB 8929), Arthrobacter roseoparaffinus (ATCC 15584), Bacillus subtilis (ATCC 15841), Brevibacterium butanicum (ATCC 21196), Brevibacterium healii (ATCC 15527), Brevibacterium ketoglutamicum (ATCC 21004), Brevibacterium paraffinoliticum (NCIB 11160); Corynebacterium fujiokense (ATCC 21496), Mycobacterium petroleophilum (ATCC 21497), Mycobacterium smegmatis (ATCC 19420), Nocardiopsis asteroides (ATCC 21943), Rhodococcus rhodochrous (NCIB 11273), Nocardia opaca (NCIB 9409), Rhodococcus sp. (ATCC 21337), Pseudomonas diminuta (NCIB 9393) or Pseudomonas lemoignei (NCIB 9947).
Claim 8
Dependent Claim
53 words
A process according to claim 1 wherein the α-aryloxypropionic acid is of formula II ##STR17## wherein Z and Y each represent fluorine, chlorine, bromine, iodine or hydrogen or a trifluoromethyl, difluoromethyl or chlorodifluoromethyl group provided that at least one of Z and Y is a halogenomethyl group and R represents a carboxyl group.
Claim 9
Dependent Claim
21 words
A process according to claim 1 wherein the process is applied to 2[4(5-trifluoromethylpyridyl-2-oxy)phenoxy]propionic acid or 2[4(3-chloro-5-trifluoromethylpyridyl-2-oxy)phenoxy]propionic acid or an ester thereof.
Claim 10
Dependent Claim
33 words
A process according to claim 1 wherein the α-aryloxypropionic acid is of formula III ##STR18## wherein B, D, J, U and V each represent hydrogen or halogen and R is a carboxyl group.
Claim 11
Dependent Claim
30 words
A process according to claim 9 wherein one of B and D is chloro, and the other hydrogen, U is hydrogen or 2-fluoro and J and U each represent hydrogen.
Claim 12
Dependent Claim
23 words
A process according to claim 1 wherein the enzyme is immobilised and contained in a column through which the [S] enantiomer is passed.
Claim 13
Dependent Claim
23 words
A process according to claim 1 wherein the [S] enantiomer is provided with the corresponding [R] enantiomer in the form of the racemate.
Claim 14
Dependent Claim
25 words
A process according to claim 1 wherein the product of the stereospecific inversion is in the form of free acid and this is subsequently esterified.
References Cited (Backward Citations)
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| 3.5 Years (Year 4) | 1989-01-20 | 1989-07-22 | 1990-01-21 | $2000.00 | Window Closed / Lapsed |
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