Benzyl chloroformate → Benzyl-4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-1-azepinecarboxylate
Reaction equation
C([N:8]1[CH2:14][CH2:13][C:12]([CH:15]=[O:16])=[C:11]([Cl:17])[CH2:10][CH2:9]1)C1C=CC=CC=1.Cl[C:19]([O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:20]>>[CH2:22]([O:21][C:19]([N:8]1[CH2:14][CH2:13][C:12]([CH:15]=[O:16])=[C:11]([Cl:17])[CH2:10][CH2:9]1)=[O:20])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
Procedure
This compound was prepared from 40 gm (0.16 mol) of 1-benzyl-4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-azepine and 34.2 gm (0.20 mol) of benzyl chloroformate analogous to Example G.
Sources & evidence
- ORD record
- ord-9a536298f3804d7b81bbb6000fdb9057
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04414225
Reaction notes
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