Hydrochloric Acid → 5-Hydroxybenzo[b]thiophene-3-carboxylic acid
Reaction equation
C1(S([O:10][C:11]2[CH:22]=[CH:21][C:14]3[S:15][CH:16]=[C:17]([C:18]([OH:20])=[O:19])[C:13]=3[CH:12]=2)(=O)=O)C=CC=CC=1.Cl>[OH-].[Na+]>[OH:10][C:11]1[CH:22]=[CH:21][C:14]2[S:15][CH:16]=[C:17]([C:18]([OH:20])=[O:19])[C:13]=2[CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
A solution of 100 mg (0.3 mmol) of the above obtained 5-benzenesulfonyloxybenzo[b]thiophene-3-carboxylic acid (2) in 1.2 ml of 1N sodium hydroxide was stirred at 40° C. for 8 hours. Hydrochloric acid (1N, 1.2 ml) was added thereto and the precipitated crystals were filtered, washed with water and dried to give 58 mg of 5-hydroxybenzo[b]thiophene-3-carboxylic acid (1). Yield 96.6%.
Workup
- filtrationthe precipitated crystals were filtered
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-76e45c3dcff243a1b4df881a3049080c
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506789B2
Reaction notes
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