Diallylamine → HCID 178418281, compound
Reaction equation
[C:1]([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]2[CH:16]=[CH:15][C:14]([CH2:17]Cl)=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)(=[O:3])[CH3:2].[CH2:19]([NH:22][CH2:23][CH:24]=[CH2:25])[CH:20]=[CH2:21]>>[C:1]([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]2[CH:16]=[CH:15][C:14]([CH2:17][N:22]([CH2:23][CH:24]=[CH2:25])[CH2:19][CH:20]=[CH2:21])=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)(=[O:3])[CH3:2]Participants
3
Procedure
from trans-O-acetyl-4-(4-chloromethylphenyl)-cyclohexanol and diallylamine. Colourless oil.
Sources & evidence
- ORD record
- ord-2c57a2e6edd64e5e962d5636e0b02f36
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05726205
Reaction notes
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