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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597690생성일: 2026년 10월 26일

N,N-Dimethylaniline → 2-Tert-butoxycarbonyloxyimino-2-(1-naphthyl)acetonitrile

https://huagongshe.com/reaction/597690

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물DiphosgeneHCID 10426—
반응물2-Chlorocarbonyloxyimino-2-(1-naphthyl)acetonitrileHCID 54347396—
반응물2-Hydroxyimino-2-(1-naphthyl)acetonitrileHCID 73680448—
용매BenzeneHCID 241—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
용매tert-ButanolHCID 6386—
생성물2-Tert-butoxycarbonyloxyimino-2-(1-naphthyl)acetonitrileHCID 53789987—

반응 단계

A solution of 2-hydroxyimino-2-(1-naphthyl)acetonitrile (7.0 g.) and dimethylaniline (12.0 g.) in toluene (100 ml.) was added dropwise, under ice-cooling, to a solution of trichloromethyl chloroformate (phosgene dimer) (3.56 g.) in benzene (30 ml.). The mixture was stirred for 3 hours at the same temperature and allowed to stand overnight. A solution of tert-butyl alcohol (11.1 g.) and pyridine (12 ml.) in toluene (20 ml.) was added dropwise, under ice-cooling, to the resultant mixture containing 2-chlorocarbonyloxyimino-2-(1-naphthyl)acetonitrile. The mixture was stirred for 6 hours at the same temperature and allowed to stand overnight. The reaction mixture was then washed with water, 1N hydrochloric acid, water, a sodium bicarbonate aqueous solution and water, and dried over magnesium sulfate. The solution was concentrated under reduced pressure and n-hexane and methanol were added to the residue. The mixture was allowed to stand in a refrigerator and the precipitated crystals were collected by filtration and recrystallized twice from methanol to give 2-tert-butoxycarbonyloxyimino-2-(1-naphthyl)acetonitrile (3.3 g.), mp 90° to 92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04014915
출처 데이터셋uspto-grants-1977_03
ORD IDord-e723dae864d24c19bf32dddbd5d5fe61
출처 메모uspto-grants-1977_03