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HRID 596225作成日:2026年10月27日

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

https://huagongshe.com/reaction/596225

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物DiphosgeneHCID 10426—
反応物2-Chlorocarbonyloxyimino-2-(1-naphthyl)acetonitrileHCID 54347396—
反応物2-Hydroxyimino-2-(1-naphthyl)acetonitrileHCID 73680448—
溶媒BenzeneHCID 241—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
溶媒tert-ButanolHCID 6386—
生成物2-Tert-butoxycarbonyloxyimino-2-(1-naphthyl)acetonitrileHCID 53789987—

反応手順

A solution of 2-hydroxyimino-2-(1-naphthyl)acetonitrile (7.0 g.) and dimethylaniline (12.0 g.) in toluene (100 ml.) was dropwise added 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. To the resultant mixture containing 2-chlorocarbonyloxyimino-2-(1-naphthyl)acetonitrile was dropwise added a solution of tert-butyl alcohol (11.1 g.) and pyridine (12 ml.) in toluene (20 ml.) under ice-cooling, and the mixture was stirred for 6 hours at the same temperature and allowed to stand overnight. The reaction mixture was in turn 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 to the residue were added n-hexane and methanol. 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04010178
出典データセットuspto-grants-1977_03
ORD IDord-9cc39cbc42fc430a9f344a74b6ad89c0
出典メモuspto-grants-1977_03