Benzylamine → 2-Benzylamino-6,7-dimethoxy-1,2,3,4-tetrahydronaphthalene
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH2:9][C:8](=O)[CH2:7][CH2:6]2.[CH2:16]([NH2:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:16]([NH:23][CH:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=2)[CH2:9]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
3
Procedure
The title compound is prepared analogously to Example L by reacting 6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-one with benzylamine. Mp: 237°-238° C.
Sources & evidence
- ORD record
- ord-f3af084c18304d718699d174787c2a88
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04584293
Reaction notes
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