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HRID 1505576作成日:2026年10月26日

Water → Hexahydrofuro[2,3-b]furan-3-yl acetate

https://huagongshe.com/reaction/1505576

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物Hexahydrofuro(2,3-b)furan-3-olHCID 9898832—
溶媒DichloromethaneHCID 6344—
生成物Hexahydrofuro[2,3-b]furan-3-yl acetateHCID 2186902290.7%

反応条件

温度2.5 °C

反応手順

Hexahydrofuro[2,3-b]furan-3-ol (IV, 60 g) was dissolved in dichloromethane (300 mL) and cooled to 0-5° C. To the cooled solution triethylamine (58.2 g), N,N-dimethylaminopyridine (1.12 g) was added, acetic anhydride (56.5 g) was added for 30-60 minutes at the same temperature, the mass temperature was raised to 25-35° C. and stirred for 2-4 hours. After completion of reaction the mass was cooled to 10-20° C., water (120 mL) was added, stirred for 30 minutes, separated the organic layer, washed with 10% sodium chloride solution (120 mL) and distilled out dichloromethane to get title compound (yield 72 g). Further, the product was purified by fractional distillation to get pure Hexahydrofuro[2,3-b]furan-3-yl acetate III (yield 54 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09216990B2
出典データセットuspto-grants-2015_12
ORD IDord-cca1ab0112f444b48d561ee32f866e66
出典メモuspto-grants-2015_12