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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59693생성일: 2026년 10월 23일

Potassium bisulfate → (4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-one

https://huagongshe.com/ko/reaction/59693

반응식

참여 물질

역할이름HCID투입량
반응물Potassium bisulfateHCID 516920—
반응물(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
반응물5-phenylpentanoyl ChlorideHCID 10965460—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-oneHCID 1078315683%

반응 조건

온도-78 °C

반응 단계

To a stirring solution consisting of (S)-4-benzyloxazolidin-2-one (0.9 g, 5.08 mmol) in THF (20 mL) at −78° C. was slowly added n-butyllithium solution (3.5 mL, 5.6 mmol, 1.6 M solution in hexane). The reaction mixture was stirred at −78° C. for two hours, after which time 5-phenylpentanoyl chloride (1 g, 5 mmol, prepared by treatment of 5-phenylpentanoic acid with oxalyl chloride and catalytic DMF) was slowly added. The reaction mixture was stirred at −78° C. for two hours and was then allowed to rise to room temperature overnight. The reaction mixture was acidified with 5% KHSO4 and extracted twice with ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by silica gel chromatography. Elution with ethyl acetate-heptane (25:75 v/v) afforded the title compound (1.4 g, 82%) as a clear oil; TLC Rf 0.40 (solvent system: 25:75 v/v ethyl acetate-heptane); MS (ESI+) m/z 337.4 (M+H)+, 360.2 (M+Na)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440919B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8c0a011ccf214c169e2ed2ad5abd4a0c
출처 메모uspto-grants-2016_09