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HRID 57379作成日:2026年10月26日

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

https://huagongshe.com/reaction/57379

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物LithiumHCID 3028194—
反応物(S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-oneHCID 90414714—
溶媒Diethyl EtherHCID 3283—
生成物(S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-oneHCID 9041663488.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434719B2
出典データセットuspto-grants-2016_09
ORD IDord-d647900c07fc4ddaafa5eae26d9861a6
出典メモuspto-grants-2016_09