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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434303생성일: 2026년 10월 26일

3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)- → (S)-4-[4-(4-Fluoro-benzoyl)-piperidin-1-ylmethyl]-2,2-dimethyl-oxazolidine-3-carboxylic Acid tert-Butyl Ester

https://huagongshe.com/reaction/434303

반응식

참여 물질

역할이름HCID투입량
반응물3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)-HCID 178792—
반응물4-(4-Fluorobenzoyl)piperidineHCID 2724440—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(S)-4-[4-(4-Fluoro-benzoyl)-piperidin-1-ylmethyl]-2,2-dimethyl-oxazolidine-3-carboxylic Acid tert-Butyl EsterHCID 68809475—

반응 단계

To a solution of (4-fluoro-phenyl)-piperidin-4-yl-methanone (3.5 g, 17 mmol) in dry tetrahydrofuran (50 ml) is added (R)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (3.9 g, 17 mmol) and sodium triacetoxyborohydride (5.4 g, 25 mmol), and the reaction mixture stirred for 18 hours at ambient temperature. The reaction mixture is filtered and the solvent evaporated to give a white solid. The solid is taken up in dichloromethane (50 ml) and washed with saturated sodium bicarbonate solution (50 ml), water (2×50 ml) and brine (50 ml). The organic phase is dried over magnesium sulphate and evaporated to afford the product, [MH]+420.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06670379B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-bcb2009a4e644e87a58309e501982678
출처 메모uspto-grants-2003_12