Cyclohexylamine → 3-chloro-N-cyclohexylbenzamide
Reaction equation
[CH:1]1([NH2:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:8][C:9]1[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12](Cl)=[O:13]>>[Cl:8][C:9]1[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12]([NH:7][CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:13]Participants
3
Procedure
Employing 0.19 g (1.9 mmol) of cyclohexylamine and 0.51 g, (2.9 mmol) of 3-chloro-benzoyl chloride in the procedure described above and elution with CHCl3/MeOH/Et3N (9.8:0.1:0.1) gave white crystals in 70% yield.
Workup
- washelution with CHCl3/MeOH/Et3N (9.8:0.1:0.1)
- customgave white crystals in 70% yield
Sources & evidence
- ORD record
- ord-388c45c4d0e04b55840efcf5cbffab1e
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975288B2
Reaction notes
Loading…