Pyrrolidine → Methanone, [3-nitro-4-(1-pyrrolidinyl)phenyl]phenyl-
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1Cl)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:8])([O-:3])=[O:2].[NH:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1>>[N+:1]([C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1[N:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:8])([O-:3])=[O:2]Participants
3
Procedure
3-Nitro-4-chloro-benzophenone is reacted with pyrrolidine as described in Examples 7 or 8 to obtain 3-nitro-4-pyrrolidino-benzophenone with a yield of 95%. The crystalline product melts at 89.5° - 90.5°C.
Sources & evidence
- ORD record
- ord-ff1c6a8d5115441294441393e73d69fa
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03957777
Reaction notes
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