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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34738생성일: 2026년 10월 24일

Benzo(B)Thiophene → 2-(Dimethoxyacetyl)benzothiophene

https://huagongshe.com/ko/reaction/34738

반응식

참여 물질

역할이름HCID투입량
반응물Benzo(B)ThiopheneHCID 7221—
반응물N-(dimethoxyacetyl)morpholineHCID 21298597—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-(Dimethoxyacetyl)benzothiopheneHCID 14276932—

반응 단계

A solution of benzothiophene (7.11 g., 0.053 mol) in 120 ml. dry THF was cooled to 0°. Butyl lithium (35.3 ml. of 1.5M in hexane, 0.053 mol) was added dropwise, maintaining 0°-5°, and the mixture then warmed to ambient temperature for 1.25 hours, cooled to -75° C. and N-(dimethoxyacetyl)morpholine (10.0 g., 0.053 mol) in 50 ml. dry THF added dropwise maintaining -75° to -70°. The reaction was quenched by adding to 300 ml. saturated NH4Cl and 300 ml. ether. The organic layer was separated, washed with brine, dried over MgSO4 and stripped to an oil, 14 g., which was distilled to yield purified title product, 8.00 g., bp 137°-139°/0.25 mm.; tlc Rf 0.23 (6:1 hexane:ethyl acetate), 0.47 (2:1 hexane:ethyl acetate); 1H-nmr 3.6 (s, 6H), 5.2 (s, 1H), 7.3-7.6 (m, 2H), 7.8-8.05 (m, 2H), 8.4 (s, 1H), tlc Rf 0.31 (4:1 hexane:ethyl acetate), 0.47 (2:1 hexane:ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762921
출처 데이터셋uspto-grants-1988_08
ORD IDord-92c875558a0a424189ef189c8a798b96
출처 메모uspto-grants-1988_08