Reaction #9738

ord-01fd9acbd4244adfb8428d8144a29522

Reaction equation

CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
Ethyl 3-methyl-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate
CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
ethyl 3-methyl-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate
CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
intermediate 35
CCOC(=O)c1sc(-c2ccc(C(F)(F)F)cc2)cc1C
ethyl 3-methyl-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate
[Na+].[O-][Br+2]([O-])[O-]
sodium bromate
O=S([O-])O.[Na+]
sodium bisulfite
Cc1sc(-c2ccc(C(F)(F)F)cc2)cc1CO
title compound
Cc1sc(-c2ccc(C(F)(F)F)cc2)cc1CO
{2-methyl-5-[4-(trifluoromethyl)phenyl]thien-3-yl}methanol

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherquenched with 1M sodium thiosulfate solution
  2. 2
    Extractionextracted with ethyl acetate
  3. 3
    Washwashed with water, sodium thiosulfate
  4. 4
    Dryingdried with brine and over MgSO4
  5. 5
    Concentrationconcentrated

Procedure

Ethyl 3-methyl-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate (intermediate 35, 0.100 g) and sodium bromate (0.144 g) were suspended in a mixture of cyclohexane and water (1:1 v/v, 4 ml). To this was added a solution sodium bisulfite (0.99 g) in water (1 ml). The mixture was stirred for 2 hours, quenched with 1M sodium thiosulfate solution, then extracted with ethyl acetate. The organic layer was taken and washed with water, sodium thiosulfate and dried with brine and over MgSO4 and concentrated to give the title compound as a white crystalline solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091237B2uspto-grants-2006_08