Methanol → Methyl 2-bromo-3-methylbutanoate

HRID 36228

反応式

HRID 36228 の反応式
[Br:1][CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([OH:5])=[O:4].[CH3:9]O>>[Br:1][CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([O:5][CH3:9])=[O:4]

参加物

3

実験手順

2-Bromo-3-methylbutyric acid (3.65 g, 20 mmole) was esterified in refluxing methanol containing 2 mL concentrated sulfuric acid for 22 hours. After cooling to room temperature, volatiles were evaporated and the residue was taken up in 50 mL of water and extracted with Et2O. The ether layer was washed with 5% aq. NaHCO3, water brine, and dried over Na2SO4. The desired material was obtained after filtration and removal of volatiles; homogeneous by TLC in 4/1 hexane/EtOAc.

後処理

  1. customvolatiles were evaporated
  2. extractionextracted with Et2O
  3. washThe ether layer was washed with 5% aq. NaHCO3, water brine
  4. dry with materialdried over Na2SO4

出典と根拠

ORDレコード
ord-98c0c321d20e4334998dacb0a35817c2
出典データセット
uspto-grants-1995_05
特許番号
US05411980

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