Sodium Hydroxide → 2-(4-Bromothiophen-2-yl)acetic acid
Reaction equation
[OH-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH2:9][C:10]([O:12]CC)=[O:11])[S:7][CH:8]=1>>[Br:3][C:4]1[CH:5]=[C:6]([CH2:9][C:10]([OH:12])=[O:11])[S:7][CH:8]=1Participants
3
Procedure
12 ml of 10% aqueous sodium hydroxide solution was added to the 4.94 g (19.8 mmol) of ethyl 4-bromo-2-thiopheneacetate and stirring carried out for 5 hours at 90° C. The reaction liquid was then cooled and extracted with ether. The aqueous layer was neutralized with hydrochloric acid, extracted with ether, then dried and concentrated. 4.24 g (19.1 mmol, 96%) of 4-bromo-2-thiopheneacetic acid was obtained.
Workup
- customThe reaction liquid
- temperaturewas then cooled
- extractionextracted with ether
- extractionextracted with ether
- customdried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-e9db741ce31f49bcaddc0e681c0b7856
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06184245B2
Reaction notes
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