Ethyl Acetate → HCID 57158131、化合物

HRID 2253565

反応式

HRID 2253565 の反応式
[OH:1][C@@H:2]([CH3:10])[C@@H:3]([CH3:9])[C:4]([O:6][CH2:7][CH3:8])=[O:5].I(O[CH3:15])(=O)=O.[H-].[Na+].C(OCC)(=O)C>CN(C)C=O>[CH3:15][O:1][C@@H:2]([CH3:10])[C@@H:3]([CH3:9])[C:4]([O:6][CH2:7][CH3:8])=[O:5]

参加物

6

実験手順

Ethyl (2R, 3S)-3-hydroxy-2-methylbutyrate (8.20 g) and methyl iodate (78.0 g) were dissolved in N,N-dimethylformamide (150 ml). To this solution was added sodium hydride (about 60% in oil, 2.46 g) little by little with ice cooling and the mixture was stirred for 1 hour with ice cooling. The reaction mixture was poured into ethyl acetate (300 ml) and the mixture was stirred for 10 minutes. Insoluble materials were filtered off and the filtrate was washed 3 times with water. The organic layer was dried, concentrated and distilled under reduced pressure (b.p. 80° C./30 mmHg) to obtain ethyl (2R, 3S)-3-methoxy-2-methylbutyrate (6.87 g).

後処理

  1. stirringthe mixture was stirred for 10 minutes
  2. filtrationInsoluble materials were filtered off
  3. washthe filtrate was washed 3 times with water
  4. customThe organic layer was dried
  5. concentrationconcentrated
  6. distillationdistilled under reduced pressure (b.p. 80° C./30 mmHg)

出典と根拠

ORDレコード
ord-e9b8d2372f61430f882f6799184a0467
出典データセット
uspto-grants-1993_08
特許番号
US05232853

関連ノート

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