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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57379생성일: 2026년 10월 25일

Ammonia → (S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one

https://huagongshe.com/reaction/57379

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물LithiumHCID 3028194—
반응물(S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-oneHCID 90414714—
용매Diethyl EtherHCID 3283—
생성물(S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-oneHCID 9041663488.1%

반응 단계

To liquid ammonia at −50° C. under argon was slowly added a solution of (S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one (627 mg) (200 mg, 0.784 mmol) in diethylether (10 mL). Lithium (pellets; 54.4 mg, 7.84 mmol) were added in three portions. The reaction mixture became green then dark greenish blue over ˜10 min. The mixture was stirred for additional 15 min and then quenched slowly by the addition of saturated aqueous ammonium chloride solution (3 mL). The mixture was allowed to warm slowly to room temperature. The residue was diluted with diethylether (20 mL) and water (10 mL). The separated aqueous layer was extract with ether (2×25 mL) and DCM (3×20 mL). The DCM and ether layers were separately concentrated under reduced pressure. The residues were dissolved in DCM and combined. The organic layer was dried over magnesium sulfate, filtered off and concentrated under reduced pressure providing crude (S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one (114 mg) as a colorless solid, which was directly used without further purification. MS m/z 166.1 (M+H)+; Rt-0.37 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d647900c07fc4ddaafa5eae26d9861a6
출처 메모uspto-grants-2016_09