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GB460647A - Improvements in insecticides - Google Patents

Improvements in insecticides

Info

Publication number
GB460647A
GB460647A GB12570/35A GB1257035A GB460647A GB 460647 A GB460647 A GB 460647A GB 12570/35 A GB12570/35 A GB 12570/35A GB 1257035 A GB1257035 A GB 1257035A GB 460647 A GB460647 A GB 460647A
Authority
GB
United Kingdom
Prior art keywords
carbinol
chloroform
trichlormethyl
monochloracetate
neutralized
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
GB12570/35A
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.)
WOLFGANG VON LEUTHOLD
Original Assignee
WOLFGANG VON LEUTHOLD
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 WOLFGANG VON LEUTHOLD filed Critical WOLFGANG VON LEUTHOLD
Publication of GB460647A publication Critical patent/GB460647A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/04Oxygen or sulfur attached to an aliphatic side-chain of a carbocyclic ring system

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Trichlormethyl - p - chlorphenyl carbinol is obtained by reacting chloral with chlorbenzol in presence of aluminium chloride, at low temperature. The reaction mixture is poured on ice and the oil layer washed, neutralized with soda, and fractionally distilled in vacuo. Trichlormethyl - p - bromphenol carbinol is similarly produced from chloral and benzol bromide. The solution is poured on ice and stirred with HCl and the oil layer neutralized and distilled. The acetates may be obtained by treating the carbinols with acetic anhydride and sodium acetate, neutralizing and recrystallizing with hot alcohol and active carbon. The monochloracetate, formate and methyl ester of trichlormethyl-p-chlorphenyl carbinol may also be prepared. The substances are used as insecticides. Other insecticidal substances referred to are acetonechloroform monochloracetate (from acetone and chloracetyl chloride), trichlormethyl - ethylmethyl carbinol (from methylethyl ketone and chloroform), trichlormethylisopropyl carbinol (from isobutylaldehyde and chloroform), and trichlormethylphenyl carbinol (from benzaldehyde and chloroform).ALSO:The active ingredients of insecticides consist of carbinols produced by reaction of chloral on chlorbenzol or brombenzol in presence of aluminium chloride as a catalyst, ethers or esters of these carbinols, acetone chloroform or its ethers or esters, or close homologues of these. The substances may be used as solutions or emulsions, or mixed with inert powders. Trichloromethyl - p - chlorophenyl carbinol is obtained by reacting chloral with chlorbenzol in presence of aluminium chloride at low temperature. After reaction, the solution is poured on ice and the oil layer washed, neutralized with soda and fractionally distilled in vacuo. The carbinol may be heated with acetic anhydride and sodium acetate, cooled, mixed with water to produce a precipitate of the acetate which is neutralized and recrystallized with hot alcohol and active carbon. The monochloracetate, formate and methyl ester may also be produced, also the corresponding trichloromethyl-p-bromphenol carbinol and its esters and ethers. Other active substances specified are acetonechloroformacetate, acetonechloroform monochloracetate (from acetone and chloracetylchloride), trichlorisopropanol, trichlormethyl-ethylmethyl carbinol (from methylethyl ketone and chloroform), trichlormethylisopropyl carbinol (from isobutyl aldehyde and chloroform), trichlormethylphenyl carbinol (from benzaldehyde and chloroform), and trichlormethylphenyl carbinol acetate.
GB12570/35A 1934-04-26 1935-04-26 Improvements in insecticides Expired GB460647A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE460647X 1934-04-26

Publications (1)

Publication Number Publication Date
GB460647A true GB460647A (en) 1937-02-01

Family

ID=6539759

Family Applications (1)

Application Number Title Priority Date Filing Date
GB12570/35A Expired GB460647A (en) 1934-04-26 1935-04-26 Improvements in insecticides

Country Status (1)

Country Link
GB (1) GB460647A (en)

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