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

HRID 57379
ノート
印刷プレビュー

反応式

HRID 57379 の反応式
N.C([N:9]1[C@@H:13]([C@@H:14]([CH3:18])[CH:15]([F:17])[F:16])[CH2:12][O:11][C:10]1=[O:19])C1C=CC=CC=1.[Li]>C(OCC)C>[F:17][CH:15]([F:16])[C@@H:14]([C@H:13]1[CH2:12][O:11][C:10](=[O:19])[NH:9]1)[CH3:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 222AmmoniaHCID 3028194LithiumHCID 90414714(S)-3-benzyl-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one

生成物 1

HCID 90416634(S)-4-((R)-1,1-difluoropropan-2-yl)oxazolidin-2-one収率 88.1%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

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.

後処理

  1. customquenched slowly by the addition of saturated aqueous ammonium chloride solution (3 mL)
  2. additionThe residue was diluted with diethylether (20 mL) and water (10 mL)
  3. extractionThe separated aqueous layer was extract with ether (2×25 mL) and DCM (3×20 mL)
  4. concentrationThe DCM and ether layers were separately concentrated under reduced pressure
  5. dissolutionThe residues were dissolved in DCM
  6. dry with materialThe organic layer was dried over magnesium sulfate
  7. filtrationfiltered off
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-d647900c07fc4ddaafa5eae26d9861a6
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434719B2

反応ノート

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