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HRID 53351생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/53351

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 번호US05618949
출처 데이터셋uspto-grants-1997_04
ORD IDord-0811c857f5db4ea5a7e911d4b6395759
출처 메모uspto-grants-1997_04