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HRID 647456생성일: 2026년 10월 26일

Toluene → alpha-Cypermethrin 1-Epimeric Mixture

https://huagongshe.com/reaction/647456

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acidHCID 41507—
반응물O-(p-toluenesulfonyl)-m-phenoxymandelonitrileHCID 12945136—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물alpha-Cypermethrin 1-Epimeric MixtureHCID 980197797.3%

반응 조건

온도70 °C

반응 단계

Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (199 g, 0.95 M) was added to a solution of potassium carbonate (65.6 g, 0.475 M) in water (450 ml). Toluene (900 ml), tetra-n-butylammonium bromide (13.5 g, 0.05 M) and alpha-cyano-3-phenoxybenzyl p-toluenesulphonate (341 g, 0.9 M; prepared as described in A above) were added to the stirred mixture which was then heated at 70° C. for 3 hours. The mixture was cooled to ambient temperature and the organic phase was separated off, washed with aqueous potassium carbonate solution (2×200 ml) and water (2×200 ml), evaporated and degassed under vacuum to leave cis-alpha-cyano-3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate as a pale amber oil (364 g, 97.3%), containing less than 1% trans-isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04409150
출처 데이터셋uspto-grants-1983_10
ORD IDord-bb5b25184ed94f6b82d54a5d9de5e618
출처 메모uspto-grants-1983_10