Carbon Dioxide → 9-Benzoyl-1,2,3,4-tetrahydrocarbazole-3-carboxylic acid
Reaction equation
[C:1]([N:9]1[C:21]2[CH2:20][CH2:19][C:18](C(O)=O)([C:22]([OH:24])=[O:23])[CH2:17][C:16]=2[C:15]2[C:10]1=[CH:11][CH:12]=[CH:13][CH:14]=2)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)=O>>[C:1]([N:9]1[C:21]2[CH2:20][CH2:19][CH:18]([C:22]([OH:24])=[O:23])[CH2:17][C:16]=2[C:15]2[C:10]1=[CH:11][CH:12]=[CH:13][CH:14]=2)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
9-Benzoyl-1,2,3,4-tetrahydrocarbazole-3,3-dicarboxylic acid (3.7 g.) was heated at 170°-200°C., till carbon dioxide evolution ceased, to give 2.5 g. of the title compound; m.p. 188°-190°C. (benzene).
Workup
- customto give 2.5 g
Sources & evidence
- ORD record
- ord-fad62b8feab84733bb3dacc706b75849
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03948939
Reaction notes
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