GB460647A - Improvements in insecticides - Google Patents
Improvements in insecticidesInfo
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/04—Oxygen 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.
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) |
-
1935
- 1935-04-26 GB GB12570/35A patent/GB460647A/en not_active Expired
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