Potassium Hydroxide → 5-(4-Acetylphenyl)-2-benzofurancarboxylic acid
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[O:17][C:16]([C:18]([O:20]CC)=[O:19])=[CH:15][C:14]=3[CH:23]=2)=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[OH-].[K+]>C(O)C>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[O:17][C:16]([C:18]([OH:20])=[O:19])=[CH:15][C:14]=3[CH:23]=2)=[CH:8][CH:9]=1)(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10A was treated with potassium hydroxide in ethanol to give 10, mp: 264°-266° C.
Sources & evidence
- ORD record
- ord-91a4f605c2434eb2bc223e64af39a369
- Source dataset
- uspto-grants-1980_07
- Patent number
- US04213998
Reaction notes
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