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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83062생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Bromo-1-benzofuranHCID 640589—
반응물1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-olHCID 67154652—

반응 조건

온도-78 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846711B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5696a1088c814c75983613d772ed75fd
출처 메모uspto-grants-2014_09