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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634016생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/634016

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 번호US09321769B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-8bda8f9d55ac4d60b951a945dda3155c
출처 메모uspto-grants-2016_04