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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1355593생성일: 2026년 10월 25일

Azobisisobutyronitrile → 5-(Bromomethyl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/1355593

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물5-Methylthiophene-2-carbonitrileHCID 312733—
용매Carbon TetrachlorideHCID 5943—
생성물5-(Bromomethyl)thiophene-2-carbonitrileHCID 1056001692.8%

반응 단계

A solution of 2-cyano-5-methylthiophene (compound 23, 3.0 g, 24 mmol), N-bromosuccinimide (Aldrich, 4.8 g, 27 mmol), and 2,2′-azobisisobutyronitrile (Aldrich, 0.4 g, 2.4 mmol) in CCl4 (Aldrich, 60 ml) was heated at its reflux temperature for 5 hours. After cooling to ambient temperature, the solvent was removed under vacuum to give a yellow oil. The oil was purified by a flash column chromatography (1:1 of hexane/ethyl acetate) to give the title compound (4.5 g, 91%). TLC: Rf 0.91 (1:1 of hexane/ethyl acetate); 1H NMR (CDCl3): δ 4.66 (s, 2H), 7.10 (d, 1H, J=3.8 Hz), 7.48 (d, 1H, J=3.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586405B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-d73e803c74c34f54b94a53a4296ad24e
출처 메모uspto-grants-2003_07