3-(4-Methoxyphenyl)prop-2-enenitrile → Benzenepropanenitrile, 4-methoxy- (9CI)

HRID 376926

반응식

HRID 376926 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([CH:7]=[CH:8][C:9]#[N:10])=[CH:5][CH:4]=1>C(O)C.[OH-].[OH-].[Pd+2]>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([CH2:7][CH2:8][C:9]#[N:10])=[CH:5][CH:4]=1

참가 물질

4

실험 절차

4-Methoxycinnamonitrile was hydrogenated in ethanol with palladium hydroxide on carbon to give 3-(4-methoxyphenyl)propionitrile. A mixture of anhydrous cerium (III) chloride (1.99 g, 8.1 mmol) in dry THF (12 mL) was stirred for 3 hours at room temperature, cooled to -78° C., and treated with MeLi (5.8 mL, 8.1 mmol). After stirring for 1 hour at -78° C. the reaction mixture was treated with 3-(4-methoxyphenyl)propionitrile (0.45 g, 2.8 mmol). The reaction mixture was stirred for 5 hours at -78° C. and then quenched with ammonium hydroxide. After warming to room temperature, the mixture was filtered, and the filtrate diluted with water and extracted with diethyl ether. The diethyl ether layer was dried over sodium sulfate and evaporated. The crude oil was purified by normal-phase chromatography to give 150 mg of 1,1-dimethyl-2-(4-methoxyphenyl)ethylamine as a light yellow oil.

출처 및 근거

ORD 기록
ord-a1fc1a0062ad43b6a0e1a6e90c4ee103
출처 데이터셋
uspto-grants-2000_02
특허 번호
US06022894

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