Hydrogen Peroxide → HCID 22915511、化合物

HRID 1377928ノート

反応式

HRID 1377928 の反応式
[C:1]([O:5][C:6]([CH2:8][CH:9]([CH2:25][CH2:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]2[CH:39]=[CH:38][C:37]([C:40]#[N:41])=[CH:36][CH:35]=2)=[CH:30][CH:29]=1)C(N1[C@@H](CC2C=CC=CC=2)COC1=O)=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH:42]O.[Li+].[OH-].C1[CH2:50][O:49]CC1>>[C:1]([O:5][C:6]([CH2:8][CH:9]([CH2:25][CH2:26][O:27][C:28]1[CH:29]=[CH:30][C:31]([C:34]2[CH:39]=[CH:38][C:37]([C:40]#[N:41])=[CH:36][CH:35]=2)=[CH:32][CH:33]=1)[C:50]([OH:49])=[O:42])=[O:7])([CH3:3])([CH3:4])[CH3:2]

参加物

5

反応条件

温度
0 °C

実験手順

To a 0° C. solution in THF (200 mL) of N-[2-tert-butyloxycarbonylmethyl-4-(4-(4-cyanophenyl)phenoxy)butanoyl]-(S)-(-)-4-benzyl-2-oxazolidinone (7.05 g, 12.7 mmol) was added 30% aqueous H2O2 (3.0 mL, 50.8 mmol) and 1M aqueous LiOH (20.3 mL, 20.3 mmol) and the reaction mixture was stirred for one hour. The reaction mixture was quenched with saturated aqueous NaHSO3 and diluted with dichloromethane. The aqueous phase was made basic with aqueous 2N NaOH and extracted twice with dichloromethane. The organic extracts were discarded and the aqueous phase was cooled to 0° C. and acidified with aqueous 2N HCl. The aqueous phase was extracted with dichloromethane and THF/dichloromethane. The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (dichloromethane/10% THF/1% methanol) gave 2-tert-butyloxycarbonylmethyl-4-[4-(4-cyanophenyl)phenoxy]butanoic acid (2.6 g, 52%).

後処理

  1. customThe reaction mixture was quenched with saturated aqueous NaHSO3
  2. additiondiluted with dichloromethane
  3. extractionextracted twice with dichloromethane
  4. extractionThe aqueous phase was extracted with dichloromethane and THF/dichloromethane
  5. dry with materialThe combined organic extracts were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-4ae1e2cafa234b70a2d6f48eb77bfff1
出典データセット
uspto-grants-1997_09
特許番号
US05665777

反応ノート

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