돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1707958생성일: 2026년 10월 27일

Tetrahydrofuran → (S)-4-isopropyl-3-(4-pentenoyl)-oxazolidin-2-one

https://huagongshe.com/reaction/1707958

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물2-Oxazolidinone, 4-(1-methylethyl)-HCID 519353—
반응물5-Chloro-1-penteneHCID 523042—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
용매Ammonium ChlorideHCID 25517—
생성물(S)-4-isopropyl-3-(4-pentenoyl)-oxazolidin-2-oneHCID 11820460—

반응 단계

To a -78° C. solution of 5.0 g of 4(4-(1-methylethyl)-2-oxazolidinone in 80 ml of tetrahydrofuran is added, dropwise, 15.5 ml of 2.5M n-butyl lithium in hexane. After stirring for 30 minutes, a solution of 4.8 g of 4-pentenyl chloride in 30 ml of tetrahydrofuran is added, dropwise, and the resulting solution is stirred at -78° C. for 3.5 hours. The reaction is diluted with aqueous ammonium chloride and diethyl ether. The organic layer is washed with water, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel, 25% ethyl acetate/petroleum ether) to give 5.8 g of the desired product as a pale yellow oil. [α]D26° =+79° (methylene chloride).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05356885
출처 데이터셋uspto-grants-1994_10
ORD IDord-e87e17fc48394bcf90ac0eaba55d3752
출처 메모uspto-grants-1994_10