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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 464749생성일: 2026년 10월 24일

Carbon Dioxide → Benzo(b)thiophene-3-carboxylic acid

https://huagongshe.com/ko/reaction/464749

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물Benzo(b)thiophene, 3-bromo-HCID 123250—
반응물MagnesiumHCID 5462224—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물Benzo(b)thiophene-3-carboxylic acidHCID 60128044%

반응 단계

A solution of 3-bromobenzothiophene (0.40 mole, (D15)) and methyl iodide (25 ml, 0.40 mole) in dry ether (400 ml) was added to a stirred mixture of magnesium turnings (24 g, 1.0 mole) and dry ether (100 ml) under nitrogen, at such a rate as to maintain a steady reflux. After the addition was complete, the reaction mixture was heated under reflux for 30 minutes and then allowed to cool to room temperature. The solution was diluted with dry toluene (500 ml) and stirred vigorously as dry carbon dioxide was bubbled through over 3 hours. The thick precipitate which formed was dissolved by the addition of dilute hydrochloric acid and the organic layer was then separated. The aqueous solution was extracted with ethyl acetate (2×300 ml) and all the organic solutions were then combined and extracted with 10% sodium carbonate solution (4×300 ml). The aqueous extracts were combined, washed with ether (2×200 ml) and then acidified with dilute hydrochloric acid. The precipitate was filtered off, washed with water and then dried under vacuum to give the title compound as a white solid (31.2 g, 44%) m.p. 171°-173°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04548948
출처 데이터셋uspto-grants-1985_10
ORD IDord-61428b7594504909ae8ab63384ed4ea3
출처 메모uspto-grants-1985_10