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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5592생성일: 2026년 10월 23일

Ammonia → 1-Benzylindole

https://huagongshe.com/ko/reaction/5592

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물IndoleHCID 798—
반응물Benzyl ChlorideHCID 7503—
반응물Sodium amideHCID 24533—
반응물SodiumHCID 5360545—
용매Diethyl EtherHCID 3283—
생성물1-BenzylindoleHCID 96913—

반응 단계

To a stirred mixture of sodium amide (prepared from 19.6 g, 0.85 mole of sodium and a few mg of Fe(NO3)3 -9H2O) and 800 mL of liquid NH3 (a dry ice condenser was used) was added a solution of 100 g (0.85 mole) of indole in 250 mL of dry ether during 15 minutes. The mixture was stirred for 30 minutes and then a solution of 107.8 g (0.85 mole) of benzyl chloride in 100 mL of dry ether was added during 30 minutes. The ammonia was allowed to evaporate overnight. The sides of the flask were washed down with MeOH and then 500 mL of H2O was added. The mixture was extracted with ether (2×500 mL). The combined ether extracts were washed with 250 mL of H2O and dried over MgSO4. The solvent was evaporated. The residue was distilled at 2 mm: fr 1, b.p. 172°- 183°, fr II, b.p. 183°-186°, 5 g; fr III, b.p. 186°-187°, 10.9 g; fr IV, b.p. 187°-191°, 121.8 g; fr V, b.p. 191°-197°, 13.9 g. Fractions III-V solidified upon standing several hours. Fraction IV had m.p. 42°-43°. Fraction III was crystallized from aqueous MeOH giving 9.9 g of colorless needles, m.p. 42.5°-43.5°. Fraction V was crystallized from aqueous MeOH giving 11.6 g of colorless needles, m.p. 43°-45.5°. The total yield was 143.3 g (81.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245046
출처 데이터셋uspto-grants-1993_09
ORD IDord-6e955e2991c44b43badb9a9ccdf6b729
출처 메모uspto-grants-1993_09