GB825875A - Substituted phenoxy-propionic acid esters and compositions containing them - Google Patents

Substituted phenoxy-propionic acid esters and compositions containing them

Info

Publication number
GB825875A
GB825875A GB1993856A GB1993856A GB825875A GB 825875 A GB825875 A GB 825875A GB 1993856 A GB1993856 A GB 1993856A GB 1993856 A GB1993856 A GB 1993856A GB 825875 A GB825875 A GB 825875A
Authority
GB
United Kingdom
Prior art keywords
radical
carbon atoms
ethyl
addition
benzyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB1993856A
Inventor
Herbert Aubrey Stevenson
Robert Frederick Brookes
Gerald Bertram Lush
James Fraser
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boots Pure Drug Co Ltd
Original Assignee
Boots Pure Drug Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to NL255148D priority Critical patent/NL255148A/xx
Priority to LU35243D priority patent/LU35243A1/xx
Priority to NL218393D priority patent/NL218393A/xx
Priority to BE558747D priority patent/BE558747A/xx
Application filed by Boots Pure Drug Co Ltd filed Critical Boots Pure Drug Co Ltd
Priority to GB1993856A priority patent/GB825875A/en
Priority to DEB45063A priority patent/DE1121403B/en
Priority to CH4765657A priority patent/CH372190A/en
Priority to FR1187748D priority patent/FR1187748A/en
Publication of GB825875A publication Critical patent/GB825875A/en
Priority to MY6100107A priority patent/MY6100107A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
    • C07C59/66Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
    • C07C59/68Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention comprises compounds of the general formula <FORM:0825875/IV (b)/1> (wherein R is an alkyl radical of at least 3 carbon atoms or a phenylalkyl, alkoxyalkyl or alkoxyalkoxyalkyl radical) and their preparation by condensing 4-chloro-2-methyl-phenol with the appropriate ester of an alpha-halopropionic acid or by esterification of alpha-(4-chloro - 2 - methyl - phenoxy) - propionic acid with the appropriate alcohol. Examples describe the preparation of the benzyl and 2-butoxy-ethyl esters by the first of these methods, the benzyl alpha-bromopropionate and 2-butoxy-ethyl alpha-bromopropionate starting materials being prepared by esterification of alpha-bromopropionic acid, and the preparation of the n-butyl, n-amyl, 2-ethyl-hexyl, 2-(2-n-butoxy-ethoxy) - ethyl, benzyl, 2 - butoxyethyl and 3:5:5-trimethylhexyl esters by the second of these methods. In the Provisional Specification no limitation is placed on the number of carbon atoms in the radical R. Specifications 573,479 and 573,510, [both in Group IV], are referred to.ALSO:Plant growth regulating compositions comprise compounds of the general formula: p <FORM:0825875/I/1> (wherein R is an alkyl radical of at least 3 carbon atoms or a phenylalkyl, alkoxyalkyl or alkoxyalkoxyalkyl radical) in admixture with carriers or diluents. The compositions may comprise an emulsifying agent and optionally an organic solvent so that emulsions may be formed on the addition of water; or they may comprise a solid inert diluent, a dispersing agent and optionally a wetting agent so that aqueous dispersions may be formed on the addition of water; or they may take the form of dusting powders in which the carrier is a powdered solid. Examples describe compositions containing esters in which R is variously 2-ethylhexyl, n-butyl, n-amyl, 2-(2-n-butoxy-ethoxy)-ethyl, benzyl, 2-n-butoxyethyl and 3: 5: 5-trimethylhexyl, solvents include acetone and xylene, emulsifying agents include a polyethylene oxide condensate of an octyl phenol with or without the addition of lauric diethanolamide, dispersing agents include a condensate of formaldehyde and an alkyl aryl sulphonate and solid diluents include kaolin. In the Provisional Specification no limitation is placed on the number of carbon atoms in the radical R. Specifications 573,479 and 573,510 [Group IV] are referred to.ALSO:Herbicidal compositions comprise compounds of the general formula <FORM:0825875/VI/1> (wherein R is an alkyl radical of at least 3 carbon atoms or a phenylalkyl, alkoxyalkyl or alkoxyalkoxyalkyl radical) in admixture with carriers or diluents. The compositions may comprise an emulsifying agent and optionally an organic solvent so that emulsions may be formed on the addition of water; or they may comprise a solid inert diluent, a dispersing agent and optionally a wetting agent so that aqueous dispersions may be formed on the addition of water; or they may take the form of dusting powders in which the carrier is a powdered solid. Examples describe compositions in which R is variously 2-ethylhexyl, n-butyl, n-amyl, 2 - (2 - n - butoxyethoxy) - ethyl, benzyl, 2 - n-butoxyethyl and 3 : 5 : 5-trimethylhexyl, solvents include acetone and xylene, emulsifying agents include a polyethylene oxide condensate of an octyl phenol with or without the addition of lauric diethanolamide, dispersing agents include a condensate of formaldehyde and an alkyl aryl sulphonate, and solid diluents include kaolin. In the Provisional Specification no limitation is placed on the number of carbon atoms in the radical R. Specifications 573,479 and 573,510, [both in Group IV], are referred to.
GB1993856A 1956-06-27 1956-06-27 Substituted phenoxy-propionic acid esters and compositions containing them Expired GB825875A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
NL255148D NL255148A (en) 1956-06-27
LU35243D LU35243A1 (en) 1956-06-27
NL218393D NL218393A (en) 1956-06-27
BE558747D BE558747A (en) 1956-06-27
GB1993856A GB825875A (en) 1956-06-27 1956-06-27 Substituted phenoxy-propionic acid esters and compositions containing them
DEB45063A DE1121403B (en) 1956-06-27 1957-06-21 Herbicides
CH4765657A CH372190A (en) 1956-06-27 1957-06-25 Process for selectively combating weeds and herbicidal composition for implementing this process
FR1187748D FR1187748A (en) 1956-06-27 1957-06-27 New herbicidal compounds, their preparation process and their applications
MY6100107A MY6100107A (en) 1956-06-27 1961-12-31 Substituted phexony-propionic acid esters and compositions containing them

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1993856A GB825875A (en) 1956-06-27 1956-06-27 Substituted phenoxy-propionic acid esters and compositions containing them

Publications (1)

Publication Number Publication Date
GB825875A true GB825875A (en) 1959-12-23

Family

ID=10137639

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1993856A Expired GB825875A (en) 1956-06-27 1956-06-27 Substituted phenoxy-propionic acid esters and compositions containing them

Country Status (7)

Country Link
BE (1) BE558747A (en)
DE (1) DE1121403B (en)
FR (1) FR1187748A (en)
GB (1) GB825875A (en)
LU (1) LU35243A1 (en)
MY (1) MY6100107A (en)
NL (2) NL255148A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0032631A2 (en) * 1980-01-16 1981-07-29 Fbc Limited Herbicidal phenoxyalkanoic acid derivatives, their preparation, compositions containing them, and their use
US4638082A (en) * 1985-02-28 1987-01-20 Societe Corial, S.A. Method of producing the p-chlorophenol ester of p-chlorophenoxyisobutyric acid
WO1995006408A1 (en) * 1993-09-01 1995-03-09 Bayer Aktiengesellschaft Root growth inhibitors
WO2010046422A2 (en) 2008-10-22 2010-04-29 Basf Se Use of auxin type herbicides on cultivated plants

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE526446A (en) *
GB573510A (en) * 1943-08-30 1945-11-23 Reginald Thomas Foster Improvements in or relating to the production of chloroaryloxyalkylcarboxylic compounds
BE465617A (en) * 1944-03-18
US2744818A (en) * 1954-12-01 1956-05-08 Pittsburgh Coke & Chemical Co Low volatile herbicidal compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0032631A2 (en) * 1980-01-16 1981-07-29 Fbc Limited Herbicidal phenoxyalkanoic acid derivatives, their preparation, compositions containing them, and their use
EP0032631A3 (en) * 1980-01-16 1981-11-11 Fbc Limited Herbicidal phenoxyalkanoic acid derivatives, their preparation, compositions containing them, and their use
US4638082A (en) * 1985-02-28 1987-01-20 Societe Corial, S.A. Method of producing the p-chlorophenol ester of p-chlorophenoxyisobutyric acid
WO1995006408A1 (en) * 1993-09-01 1995-03-09 Bayer Aktiengesellschaft Root growth inhibitors
US5672568A (en) * 1993-09-01 1997-09-30 Bayer Aktiengesellschaft Root growth inhibitors for building materials comprising monohydric alcohol esters of mecoprop
WO2010046422A2 (en) 2008-10-22 2010-04-29 Basf Se Use of auxin type herbicides on cultivated plants

Also Published As

Publication number Publication date
BE558747A (en)
MY6100107A (en) 1961-12-31
FR1187748A (en) 1959-09-15
LU35243A1 (en)
NL255148A (en)
NL218393A (en)
DE1121403B (en) 1962-01-04

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