Ammonium Chloride → (3S,5R)-5-Methyl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidine-3-carbonyl)-octanoic acid tert-butyl ester
反応式
[CH3:1][C@@H:2]1[C@H:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[O:5][C:4](=[O:13])[N:3]1[C:14](=[O:22])[CH2:15][CH2:16][C@H:17]([CH3:21])[CH2:18][CH2:19][CH3:20].C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[C:33]([O:37][C:38](=[O:41])[CH2:39]Br)([CH3:36])([CH3:35])[CH3:34].[Cl-].[NH4+]>C1COCC1>[C:33]([O:37][C:38](=[O:41])[CH2:39][C@@H:15]([C:14]([N:3]1[C@H:2]([CH3:1])[C@H:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[O:5][C:4]1=[O:13])=[O:22])[CH2:16][C@H:17]([CH3:21])[CH2:18][CH2:19][CH3:20])([CH3:36])([CH3:35])[CH3:34]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- -50 °C
実験手順
To oxazolidinone 100 (12.1 g, 0.04 mol) in THF (200 ml) at −50° C. was added NaHMDS (48 mL of a 1 M solution in THF). After 30 t-butylbromoaceate (15.6 g, 0.08 mol) was added. The solution was stirred for 4 hours at −50° C. and then warmed to room temperature. After 16 hours a saturated aqueous solution of ammonium chloride was added and the two layers separated. The aqueous phase was extracted with ether and the combined organic phases dried (MgSO4) and concentrated. Flash chromatography (9:1 hexane/EtOAc) gave the product 101 as a white solid 12 g; 72%. [α]D=30.2 (c 1 in CHCl3). 13C NMR (100 MHz; CDCl3) 176.47, 171.24, 152.72, 133.63, 128.87, 125.86, 80.85, 78.88, 55.34, 39.98, 38.77, 38.15, 37.58, 30.60, 28.23, 20.38, 20.13, 14.50, 14.28.
後処理
- temperaturewarmed to room temperature
- customthe two layers separated
- extractionThe aqueous phase was extracted with ether
- dry with materialthe combined organic phases dried (MgSO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-3479246ca5e14315af1245f5c9feb096
- 出典データセット
- uspto-grants-2003_11
- 特許番号
- US06642398B2
反応ノート
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