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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52834생성일: 2026년 10월 24일

Tetrahydrofuran → N-Cyclobutylacetyl-4-benzyl-2-oxazolidinone

https://huagongshe.com/ko/reaction/52834

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
반응물ButyllithiumHCID 178418339—
용매ChloroformHCID 6212—
생성물N-Cyclobutylacetyl-4-benzyl-2-oxazolidinoneHCID 2118075658%

반응 단계

To (S)(-)-4-benzyl-2-oxazolidinone (2.65 g, 1.8 equiv) dissolved in tetrahydrofuran (25 mL) at -78° C. was added 2.5M butyl lithium (5.98 mL, 1.8 equiv). After 5 minutes, this solution was cannulated into the above solution. The reaction mixture was allowed to come to room temperature and stirred for 2 hours. The reaction mixture was diluted with Chloroform (150 mL), washed with 10% sodium bisulfite (100 mL), dried over sodium sulfate, and concentrated under reduced pressure. The residue obtained was chromatographed on silica gel eluting with 3:2 hexane/ethyl acetate to afford the title compound in 58% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616714
출처 데이터셋uspto-grants-1997_04
ORD IDord-3a9e37f27d224dd895b0fb94db23dd32
출처 메모uspto-grants-1997_04