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HRID 647457作成日:2026年10月26日

Toluene → alpha-Cypermethrin 1-Epimeric Mixture

https://huagongshe.com/reaction/647457

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acidHCID 41507—
反応物O-(p-toluenesulfonyl)-m-phenoxymandelonitrileHCID 12945136—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物alpha-Cypermethrin 1-Epimeric MixtureHCID 980197799%

反応条件

温度70 °C

反応手順

Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (1680 g, 8.04 M) was added to a solution of potassium carbonate (555 g, 4.02 M) in water (3800 ml). Toluene (7600 ml), tetra-n-butylammonium bromide (115 g, 0.4 M) and alpha-cyano-3-phenoxybenzyl p-toluenesulphonate (2902 g, 7.65 M; prepared as in Example 1(A) above) were added to the stirred mixture which was then heated at 70° C. for 5 hours. The mixture was cooled to ambient temperature and the organic phase was separated off, washed twice with aqueous potassium carbonate solution and twice with water, evaporated and degassed under vacuum to leave cis-alpha-cyano-3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate as a yellow oil (3130 g, 99%), containing less than 1% trans-isomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04409150
出典データセットuspto-grants-1983_10
ORD IDord-4add32f706d6482bb574c4d3955c5caa
出典メモuspto-grants-1983_10