Aniline → 1,2,3,4-Tetrahydrocarbazole
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:8]1(=O)[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1>>[CH2:10]1[C:9]2[NH:1][C:2]3[C:7](=[CH:6][CH:5]=[CH:4][CH:3]=3)[C:8]=2[CH2:13][CH2:12][CH2:11]1Participants
3
Procedure
Aniline was reacted with cyclohexanone in the same way as in Example 3. Tetrahydrocarbazole was formed in a yield of 87% of the theoretical yield.
Sources & evidence
- ORD record
- ord-bcb663bf6d44472aad6c1506f0936c16
- Source dataset
- uspto-grants-1993_01
- Patent number
- US05179211
Reaction notes
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