反応式
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[C:19]([O:23][C:24]([N:26]1[C@H:30]([CH:31]=[O:32])[CH2:29][O:28][C:27]1([CH3:34])[CH3:33])=[O:25])([CH3:22])([CH3:21])[CH3:20].[F:35][C:36]1[CH:41]=[C:40]([CH2:42][CH2:43][N+:44]([O-:46])=[O:45])[CH:39]=[C:38]([F:47])[CH:37]=1>O1CCCC1>[C:19]([O:23][C:24]([N:26]1[C@@H:30]([C@@H:31]([OH:32])[C@@H:43]([N+:44]([O-:46])=[O:45])[CH2:42][C:40]2[CH:41]=[C:36]([F:35])[CH:37]=[C:38]([F:47])[CH:39]=2)[CH2:29][O:28][C:27]1([CH3:34])[CH3:33])=[O:25])([CH3:22])([CH3:21])[CH3:20]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
Add tetrabutylammonium fluoride in 5 minutes (50 mL, 50 mmol, 1.0 M solution in tetrahydrofuran) to a solution of (S)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester (200 g, 873.362 mmol) and 1,3-difluoro-5-(2-nitroethyl)-benzene (164 g, 877.005 mmol) in tetrahydrofuran (1.2 L) at 8° C. Allow to warm to room temperature and stir for 14 hours. Partition between ethyl acetate (4 L) and saturated aqueous sodium chloride (1.5 L). Wash the organic layer with saturated aqueous ammonium chloride, saturated aqueous sodium chloride, water, dry (magnesium sulfate), filter and concentrate to give 379 g of a crude waxy pale orange solid. Recrystallize in dichloromethane/hexanes to give the title compound (137.15 g, 37.7%).
後処理
- customPartition between ethyl acetate (4 L) and saturated aqueous sodium chloride (1.5 L)
- washWash the organic layer with saturated aqueous ammonium chloride, saturated aqueous sodium chloride, water
- dry with materialdry (magnesium sulfate)
- filtrationfilter
- concentrationconcentrate
- customto give 379 g of a crude waxy pale orange solid
- customRecrystallize in dichloromethane/hexanes
出典と根拠
- ORDレコード
- ord-74539357565a492c9ff90b62911522ae
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07745438B2
関連ノート
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