Pentanoic Acid → (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one

HRID 349793

反応式

HRID 349793 の反応式
[C:1]([OH:7])(=O)[CH2:2][CH2:3][CH2:4][CH3:5].CCN(CC)CC.CC(C)(C)C(Cl)=O.[CH3:22][C@H:23]1[C@@H:27]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[O:26][C:25](=[O:34])[NH:24]1.[Li+].[Cl-]>C1COCC1>[CH3:22][C@H:23]1[C@@H:27]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[O:26][C:25](=[O:34])[N:24]1[C:1](=[O:7])[CH2:2][CH2:3][CH2:4][CH3:5]

参加物

7

反応条件

温度
0 °C

実験手順

To a 0° C. stirred solution of valeric acid (3.83 mL, 35.2 mmol) and Et3N (14.7 mL, 106 mmol) in dry THF (175 mL) was added trimethylacetyl chloride (5.29 mL, 42.3 mmol) dropwise. The mixture was stirred at 0° C. for 1 hour and (4S,5R)-(−)-4-methyl-5-phenyl-2-oxazolidinone (7.50 g, 42.3 mmol) was added followed by LiCl (1.79 g, 42.3 mmol). The reaction was warmed to room temperature overnight with good stirring. The mixture was filtered and the filtrate was concentrated under reduced pressure. Et2O (75 mL) was added to the residue, which was washed with sat. NaHCO3 (3×40 mL), 1N HCl (3×40 mL), and brine (2×40 mL). The organic phase was dried over MgSO4, filtered and concentrated under reduced pressure to give a quantitative yield of crude product.

後処理

  1. temperatureThe reaction was warmed to room temperature overnight with good stirring
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. additionEt2O (75 mL) was added to the residue, which
  5. washwas washed with sat. NaHCO3 (3×40 mL), 1N HCl (3×40 mL), and brine (2×40 mL)
  6. dry with materialThe organic phase was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-9588e0009edb46169dab5a77c0f54ace
出典データセット
uspto-grants-2007_02
特許番号
US07179934B2

関連ノート

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