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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46752생성일: 2026년 10월 23일

Sodium Cyanide → Cypermethrin

https://huagongshe.com/ko/reaction/46752

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물3-PhenoxybenzaldehydeHCID 38284—
반응물3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic anhydrideHCID 92550—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물CypermethrinHCID 2912—

반응 단계

A 100-ml round-bottomed flask equipped with a magnetic stirrer was charged with 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylic anhydride (10 mmol), prepared as described above, 3-phenoxybenzaldehyde (10 mmol) and a mixture of alkanes (25 ml) having a boiling range of from 60° C. to 80° C. A solution of sodium cyanide (12 mmol) and tetrabutylammonium bromide (0.006 mmol) in water (3 ml) was added to the mixture in the flask at a temperature of 20° C. and stirring was continued. After 100 minutes stirring, the reaction had come to a standstill at a conversion of 3-phenoxybenzaldehyde of 98.5% and at a yield of the title ester of 98%. The mixture obtained was allowed to settle into an organic and an aqueous layer, the aqueous layer was extracted with toluene (15 ml), the extract phase obtained was added to the organic layer obtained by settling of the reaction mixture, the organic liquid thus formed, was washed with water (25 ml), the washed liquid was dried and the solvent was evaporated from the dried liquid, leaving a residue containing the title ester. The yield of this ester was 96%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175094
출처 데이터셋uspto-grants-1979_11
ORD IDord-a0c23644d7d14e22b3771975216734ff
출처 메모uspto-grants-1979_11