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HRID 440512作成日:2026年10月26日

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

https://huagongshe.com/reaction/440512

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物DihydrobenzofuranHCID 10329—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
生成物2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 279501428.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05519034
出典データセットuspto-grants-1996_05
ORD IDord-abf77135cf584e258ffec244dcfb972a
出典メモuspto-grants-1996_05