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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53348생성일: 2026년 10월 23일

Ammonium Chloride → (S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-one

https://huagongshe.com/ko/reaction/53348

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-Oxazolidinone, 4-phenyl-, (4S)-HCID 730424—
반응물(E)-pent-2-enoyl chlorideHCID 5706546—
반응물Sodium hexamethyidisilazaneHCID 45051731—
용매TetrahydrofuranHCID 8028—
생성물(S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-oneHCID 1109686328.7%

반응 조건

온도-50 °C

반응 단계

(S)-(+)-4-Phenyl-2-oxazolidinone (4.0 g, 24 mmol, Aldrich) was dissolved in dry THF (40 mL), and the solution was cooled to -50° C. and flushed with N2. Sodium hexamethyldisilazane (1.0M in THF, 25 mL, 25 mmol) was added slowly with stirring. The compound from step 7a (2.9 g, 24 mmol) was added slowly while maintaining the temperature at -50° C., and the mixture was stirred at this temperature for 1.5 hour. The mixture was allowed to warm to 0° C. and stirred for 1 hour. Saturated aqueous NH4Cl solution was added, the mixture was stirred for 10 minutes and the mixture was extracted with methylene chloride. The extract was dried over Na2SO4, filtered and the solvent was removed. The residue was chromatographed on silica gel, eluting with 2% methanol/methylene chloride, and the product was rechromatographed with 0.5% methanol/methylene chloride to give the title compound (1.69 g). MS m/ z 246 (M+H)+, 263 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618949
출처 데이터셋uspto-grants-1997_04
ORD IDord-54fbe7df9da8436eb7d74aeb74befc5f
출처 메모uspto-grants-1997_04