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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37783생성일: 2026년 10월 23일

Methanol → 1-Azabicyclo[3.2.2]nonan-4-one

https://huagongshe.com/ko/reaction/37783

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물3-QuinuclidinoneHCID 19507—
반응물Trimethylsilyldiazomethane hexaneHCID 86587183—
용매TetrahydrofuranHCID 8028—
생성물1-Azabicyclo[3.2.2]nonan-4-oneHCID 6420307—

반응 단계

An ice-cooled solution (5° C.) of (trimethylsilyl)diazomethane/hexane (2 N, 30 mL, 60 mmol; Aldrich) under nitrogen was treated dropwise with a solution of quinuclidin-3-one (7500 mg, 60 mmol) in dry tetrahydrofuran (40 mL). Methanol (20 mL) was added, and the yellow solution was warmed to room temperature, stirred for 24 hours, and quenched to colorless by addition of acetic acid. After a few minutes, saturated aqueous sodium carbonate (15 mL) was added. The organic layer was separated, and the aqueous solution was extracted with methylene chloride (3×50 mL). The combined organic layer and extracts were dried over magnesium sulfate, and concentrated in vacuo to give the titled compound. The material was used directly for next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524703B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-788482f2c86d4fcf85ad7c5a22fe736c
출처 메모uspto-grants-2013_09