Methanol → Methyl 2-bromo-3-methylbutanoate

HRID 36228

Reaktionsgleichung

Reaktionsgleichung von HRID 36228
[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]

Komponenten

3

Edukt 2

HCID 887MethanolHCID 112682-Bromoisovaleric acid

Produkt 1

HCID 228837Methyl 2-bromo-3-methylbutanoate

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-98c0c321d20e4334998dacb0a35817c2
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05411980

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