Reaktion #453136

ord-a7b02d0bff1d45a7a3200b6dadfc077f

Reaktionsgleichung

BrBr
bromine
CC(=O)O
acetic acid
CCOC(=O)c1c(C)cccc1O
ethyl 6-methyl-2-hydroxybenzoate
CC(=O)O
acetic acid
CCOC(=O)c1c(O)ccc(Br)c1C
product
CCOC(=O)c1c(O)ccc(Br)c1C
Ethyl 5-bromo-6-methyl-2-hydroxybenzoate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe organic phase is washed with water twice
  2. 2
    Einengenconcentrated in vacuo
  3. 3
    Sonstigethe residue is purified by flash chromatography (petrol ethers:ethyl acetate, 98:2 v/v)

Vorschrift

A mixture of bromine (5.05 ml, 0.099 mol) and acetic acid (15 ml) is added to a mixture of ethyl 6-methyl-2-hydroxybenzoate (17.05 g, 0.095 mol), and acetic acid (15 ml) at a temperature of 20° C. The reaction mixture is stirred at room temperature for 1 hour. The reaction mixture is diluted with water and ethyl acetate. The organic phase is washed with water twice, concentrated in vacuo and the residue is purified by flash chromatography (petrol ethers:ethyl acetate, 98:2 v/v) yielding the pure product as a yellow oil, 21.7 g, (88.2%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06127570uspto-grants-2000_10