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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485982생성일: 2026년 10월 25일

Sodium hydride → p-(1-Trifluoromethyl-heptyloxy)-benzonitrile

https://huagongshe.com/reaction/485982

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-IodobenzonitrileHCID 76467—
반응물2-Octanol, 1,1,1-trifluoro-HCID 97804—
반응물SodiumHCID 5360545—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물p-(1-Trifluoromethyl-heptyloxy)-benzonitrileHCID 15724839—

반응 단계

Into 100 ml of dry DMF containing 0.86 g of sodium hydride (purity 60%), were added dropwise 3.9 g of R-form oa 1-trifluoromethyl-heptanol, at room temperature with such a speed not causing too rapid generation of hydrogen, to prepare sodium salt (alkoxide) of R-form oa 1-trifluoromethyl-heptanol After addition was over, stirring was continued further an hour at room temperature, followed by adding thereto 4.80 g of p-iodo-benzonitrile and then refluxing for 2 hours. After cooling, the product was introduced into iced water, and extracted with hexane The hexane phase was washed subsequently with water, 1N-HCl aqueous solution and then water, followed by purifying with silica gel column to obtain 5.16 g of oily oa p-(1-trifluoromethyl-heptyloxy)- benzonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05290478
출처 데이터셋uspto-grants-1994_03
ORD IDord-242b6d19ba4c412a9d9f75a81a5fd535
출처 메모uspto-grants-1994_03