Reacción #84049

ord-195c3d7f9ab44d679c042dadfc5e6873

Ecuación de reacción

COC(=O)c1cc2ccc(Br)cc2s1
methyl 6-bromo-1-benzothiophene-2-carboxylate
[K+].[OH-]
potassium hydroxide
O=C(O)c1cc2ccc(Br)cc2s1
desired product
O=C(O)c1cc2ccc(Br)cc2s1
6-Bromo-1-benzothiophene-2-carboxylic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent is removed in vacuo
  2. 2
    FiltraciónThe resulting precipitate is filtered off with suction
  3. 3
    Lavadowashed with water
  4. 4
    Otrodried in vacuo at 50° C

Procedimiento

A solution of 4.0 g (14.8 mmol) of methyl 6-bromo-1-benzothiophene-2-carboxylate in 40 ml of a 1:1 mixture of THF and 2 N potassium hydroxide solution is stirred at room temperature for 2 h. The solvent is removed in vacuo, and the residue is acidified with concentrated hydrochloric acid. The resulting precipitate is filtered off with suction, washed with water and dried in vacuo at 50° C. 3.55 g (93.5% of theory) of the desired product are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09433614B2uspto-grants-2016_09