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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77363생성일: 2026년 10월 25일

Bromoacetonitrile → ethyl 1-(cyanomethyl)-5-methyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/77363

반응식

참여 물질

역할이름HCID투입량
반응물BromoacetonitrileHCID 11534—
반응물Sodium hydrideHCID 24758—
반응물1H-Pyrrole-2-carboxylic acid, 5-methyl-, ethyl esterHCID 96598—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물ethyl 1-(cyanomethyl)-5-methyl-1H-pyrrole-2-carboxylateHCID 8670666239.8%

반응 단계

A solution of ethyl 5-methyl-1H-pyrrole-2-carboxylate (1 g, 6.53 mmol) in anhydrous N,N-dimethylformamide (20 mL) under nitrogen at 0° C. was treated with a 60% dispersion of sodium hydride in mineral oil (392 mg, 9.79 mmol). After effervescence ceased, the reaction was treated with a solution of 2-bromoacetonitrile (1.17 g, 9.79 mmol) in N,N-dimethylformamide (2 mL). The resulting mixture was allowed to warm to room temperature and was stirred at room temperature for 30 min. At this time, the reaction was diluted with ethyl acetate (200 mL), washed with water (2×100 mL) and a saturated aqueous sodium chloride solution (2×100 mL), dried over sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (80 g silica gel column, 0-20% ethyl acetate/hexanes) afforded ethyl 1-(cyanomethyl)-5-methyl-1H-pyrrole-2-carboxylate (0.5 g, 39.8%). LC-MS calcd. for C10H13N2O2 [(M+H+] 193, obsd. 193.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841299B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a8e6857b07574fe5b2a7a3e665fe38ee
출처 메모uspto-grants-2014_09