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HRID 83062作成日:2026年10月24日

Water → 1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-ol

https://huagongshe.com/ja/reaction/83062

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Bromo-1-benzofuranHCID 640589—
反応物1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-olHCID 67154652—

反応条件

温度-78 °C

反応手順

A 2.5 M solution of n-butyllithium in hexanes (2.23 mL, 5.58 mmol) was added dropwise to a solution of 3-bromobenzofuran (1.0 g, 5.08 mmol) in THF (35 mL) at −78° C. The reaction mixture was stirred for 30 minutes at −78° C. and then a solution of 1-benzhydrylazetidin-3-one (1.2 g, 5.08 mmol, as prepared in step 1 of example FAB270) in THF (10 mL) was added dropwise at the same temperature. The mixture was allowed to warm back to room temperature overnight. Water (50 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel using petroleum ether/dichloromethane (50:50 to 0:100) as eluent. The title compound was obtained as a yellow solid (230 mg, 13%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846711B2
出典データセットuspto-grants-2014_09
ORD IDord-5696a1088c814c75983613d772ed75fd
出典メモuspto-grants-2014_09