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HRID 59693作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium bisulfateHCID 516920—
反応物(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
反応物5-phenylpentanoyl ChlorideHCID 10965460—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(4S)-4-benzyl-3-(5-phenylpentanoyl)-1,3-oxazolidin-2-oneHCID 1078315683%

反応条件

温度-78 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440919B2
出典データセットuspto-grants-2016_09
ORD IDord-8c0a011ccf214c169e2ed2ad5abd4a0c
出典メモuspto-grants-2016_09