4-Chlorobenzoyl chloride → HCID 178444846, compound
Reaction equation
[CH2:1]([NH:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25](Cl)=[O:26])=[CH:23][CH:22]=1>>[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([N:7]([C@H:8]2[CH2:13][CH2:12][C@H:11]([C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH2:10][CH2:9]2)[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[O:26])=[CH:23][CH:22]=1Participants
3
Procedure
from trans-N-hexyl-4-phenylcyclohexylamine and 4-chlorobenzoylchloride. Melting point: 105° C.
Sources & evidence
- ORD record
- ord-68de126a84664f6390125c705bbcf215
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05455273
Reaction notes
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