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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8119생성일: 2026년 10월 24일

Bromoacetonitrile → 2-((1H-Indol-4-yl)oxy)acetonitrile

https://huagongshe.com/ko/reaction/8119

반응식

참여 물질

역할이름HCID투입량
반응물BromoacetonitrileHCID 11534—
반응물Sodium hydrideHCID 24758—
반응물1H-indol-4-olHCID 75421—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-((1H-Indol-4-yl)oxy)acetonitrileHCID 1554179997%

반응 단계

A 0° C. solution of 4-hydroxyindole (20 g, 150 mmol) in 500 ml of dimethylformamide is treated with NaH (60% dispersion in mineral oil; 6.6 g, 165 mmol). After 30 minutes, bromoacetonitrile (11.5 ml, 165 mmol) is added, and the resulting mixture is allowed to slowly warm to ambient temperature and stir for 3 days. The reaction mixture is diluted with ethyl acetate and washed 3 times with H2O. The organic layer is dried over Na2SO4 and concentrated in vacuo. The crude residue is purified by normal phase HPLC (SiO2; 5% step gradient of 0 to 20% ethyl acetate in hexanes) to give 25 g of (1H-indol-4-yloxy)acetonitrile (97%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f7a1ba14ffa947f1be82f724f443f402
출처 메모uspto-grants-2006_08