GB729625A - Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer - Google Patents

Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer

Info

Publication number
GB729625A
GB729625A GB14360/53A GB1436053A GB729625A GB 729625 A GB729625 A GB 729625A GB 14360/53 A GB14360/53 A GB 14360/53A GB 1436053 A GB1436053 A GB 1436053A GB 729625 A GB729625 A GB 729625A
Authority
GB
United Kingdom
Prior art keywords
cresol
alkali
methyl
hypochlorite
odorous
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
GB14360/53A
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.)
KONINK IND MIJ VOORHEEN NOURY
Original Assignee
KONINK IND MIJ VOORHEEN NOURY
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
Application filed by KONINK IND MIJ VOORHEEN NOURY filed Critical KONINK IND MIJ VOORHEEN NOURY
Publication of GB729625A publication Critical patent/GB729625A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/363Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/367Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

2-Methyl-4-chlorophenoxyacetic acid is prepared by reacting o-cresol with an alkali metal chloracetate in alkaline solution and treating the reaction liquid at pH above 8 (with or without recovering unchanged o-cresol) with a hypochlorite. This latter step results in an odourless product. The hypochlorite (preferably sodium) may be added as a separate solution or may be formed by passing chlorine into the alkaline reaction liquid, with further addition of alkali to maintain the pH above 8. The product may if desired be separated by acidification and may be converted into salts and esters. Examples are given of the process with and without steam distillation to remove the bulk of the unchanged o-cresol. Specifications 592,827 and 683,131 are referred to.ALSO:Non-odorous solutions of alkali 2-methyl-4-chlorophenoxyacetates (containing also inorganic salts) are obtained by reacting o-cresol with an alkali chloracetate in alkaline solution and treating the reaction liquid at pH above 8 (with or without recovering unchanged o-cresol) with a hypochlorite or chlorine and alkali. The latter treatment decomposes residual o-cresol without forming chlorocresols and the product is odourless and does not cause turbidity in hard water. Examples are given of the process.
GB14360/53A 1952-05-29 1953-05-21 Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer Expired GB729625A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL729625X 1952-05-29

Publications (1)

Publication Number Publication Date
GB729625A true GB729625A (en) 1955-05-11

Family

ID=19817922

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14360/53A Expired GB729625A (en) 1952-05-29 1953-05-21 Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer

Country Status (1)

Country Link
GB (1) GB729625A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL442918A1 (en) * 2022-11-23 2024-03-11 Politechnika Poznańska Method of isolating n-bromoalkyl 4-chloro-2-methylphenoxyacetates from the post-reaction mixture using flash chromatography

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL442918A1 (en) * 2022-11-23 2024-03-11 Politechnika Poznańska Method of isolating n-bromoalkyl 4-chloro-2-methylphenoxyacetates from the post-reaction mixture using flash chromatography

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