Benzofuran-2-carboxylic acid → 2-Benzofurancarbonyl chloride
Reaction equation
S(Cl)([Cl:3])=O.[O:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH:7]=[C:6]1[C:14]([OH:16])=O>C1C=CC=CC=1>[O:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH:7]=[C:6]1[C:14]([Cl:3])=[O:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Thionyl chloride (12.5 ml) was added to a suspension of benzofuran-2-carboxylic acid (20 g) in anhydrous benzene (250 ml). The mixture was refluxed for 3 hours, then allowed to cool down to room temperature. Removal of the volatiles left the desired acid chloride (21.8 g, 98%).
Workup
- temperatureThe mixture was refluxed for 3 hours
- customRemoval of the volatiles
- waitleft the desired acid chloride (21.8 g, 98%)
Sources & evidence
- ORD record
- ord-d45c4f6c0e7346feb23031855d3cec3b
- Source dataset
- uspto-grants-1994_05
- Patent number
- US05310930
Reaction notes
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