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HRID 1378466생성일: 2026년 10월 26일

Ammonium Chloride → (4S)-4-Phenyl-3-(3-phenylprop-2-enoyl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1378466

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-Oxazolidinone, 4-phenyl-, (4S)-HCID 730424—
반응물Cinnamoyl ChlorideHCID 5354261—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(4S)-4-Phenyl-3-(3-phenylprop-2-enoyl)-1,3-oxazolidin-2-oneHCID 679769—

반응 조건

온도-78 °C

반응 단계

(S)-(+)-4-Phenyl-2-oxazolidinone (4.77 g, 29.3 mmol, Aldrich) was dissolved in dry THF (100 mL), and the solution was cooled to -78° C. and flushed with N2. n-Butyllithium (2.5M in THF, 11.7 mL, 29.3 mmol) was introduced over 10 minutes. The compound from step 8a (in 30 mL of THF) was added over 10 minutes, and the mixture was stirred at -78° C. for half an hour. The mixture was stirred as it was allowed to warm to room temperature. Saturated aqueous NH4Cl solution was added, the mixture was stirred for 10 minutes and the THF was removed under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was washed with water, 5% aqueous NaHCO3 and brine, then dried over Na2SO4. The solvent was removed to afford the title compound, which was recrystallized from ethyl acetate to give the title product (7.18 g). MS m/z 294 (M+H)+, 311 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05668164
출처 데이터셋uspto-grants-1997_09
ORD IDord-843a947afca74a3bab2b405582f63406
출처 메모uspto-grants-1997_09