Reacción #1988397

ord-a2abf8a0368644d39cf051d9aef66859

Ecuación de reacción

O=C(O)Cc1ccc(O)c(O)c1
3,4-dihydroxyphenylacetic acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cl
hydrogen chloride
CC(=O)CBr
bromoacetone
COC(=O)Cc1ccc(OCC(C)=O)c(O)c1
title compound
COC(=O)Cc1ccc(OCC(C)=O)c(O)c1
Methyl 3-hydroxy-4-(2-oxopropoxy)phenylacetate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothat described in Preparation 21

Procedimiento

Following a procedure similar to that described in Preparation 21, but using 10 g of 3,4-dihydroxyphenylacetic acid, 30 ml of absolute methanol, 20 ml of a 4N solution of hydrogen chloride in dioxane, 200 ml of anhydrous dimethylformamide, 8.74 g of bromoacetone and 8.02 g of potassium carbonate, the title compound was obtained having an Rf=0.37 (thin layer chromatography over silica gel, using a 1:2 by volume mixture of ethyl acetate and hexane as the developing solvent).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05576340uspto-grants-1996_11