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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440512생성일: 2026년 10월 25일

Carbon Dioxide → 2,3-Dihydro-1-benzofuran-7-carboxylic acid

https://huagongshe.com/reaction/440512

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물DihydrobenzofuranHCID 10329—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매HexaneHCID 8058—
생성물2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 279501428.4%

반응 단계

N,N,N',N'-Tetramethylethylenediamine (231.4 g) was added at ambient temperature to a solution of n-butyl lithium (2.5M, 800 ml) in hexane (2.5 l) followed by a solution of 2,3-dihydrobenzo[b]furan (102 g) in hexane (25 ml). The mixture was stirred under nitrogen at ambient temperature for 5 hours. The resulting suspension was added slowly to dry ice (300 g) and hexane (500 ml) under nitrogen. After stirring at ambient temperature for 16 hours, the mixture was diluted with water (2 l), and the layers separated. The aqueous layer was washed with hexane, acidified to pH 1 with concentrated hydrochloric acid, cooled and the precipitate collected by filtration. This was washed with water and dichloromethane and dried at 80° C. in vacuo to give 2,3-dihydrobenzo[b]furan-7-carboxylic acid (39.6 g), m.p. 164°-165° C. The hexane layer was filtered, dried over sodium sulphate and concentrated. On cooling, further product was obtained (32.7 g), m.p. 170° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05519034
출처 데이터셋uspto-grants-1996_05
ORD IDord-abf77135cf584e258ffec244dcfb972a
출처 메모uspto-grants-1996_05