Reacción #5146

ord-65ea4057d75b4366aba54ef2265871f0

Ecuación de reacción

C=C(C)C(=O)Cl
methacryloyl chloride
OCCOCc1csc(Br)c1
2-bromo-4-2-hydroxyethoxymethylthiophene
c1ccncc1
pyridine
CC#N
acetonitrile
O
water
C=C(C)C(=O)OCC(OC)c1csc(Br)c1
2-bromo-4-thienyl-methoxyethyl methacrylate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGAfter stirring the mixture for one hour
  2. 2
    ExtracciónThe ethyl acetate layer was extracted
  3. 3
    Concentraciónconcentrated
  4. 4
    Otropurified by column chromatography

Procedimiento

While stirring a mixture of 0.1 mol of 2-bromo-4-2-hydroxyethoxymethylthiophene, 0.1 mol of pyridine, and 100 ml of acetonitrile at a temperature of lower than 10° C., 0.1 mol of methacryloyl chloride was added dropwise to the mixture over a period of 30 minutes. After stirring the mixture for one hour, 200 ml of ethyl acetate and 200 ml of water were added to the mixture. The ethyl acetate layer was extracted, concentrated, and purified by column chromatography to provide 22.1 g of 2-bromo-4-thienyl-methoxyethyl methacrylate (5-A).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05243004uspto-grants-1993_09