Hydrochloric Acid → HCID 67301556, compound
Reaction equation
C(N[C:5](=[CH:10][C:11]1[CH:16]=[C:15]([CH3:17])[C:14]([Cl:18])=[C:13]([CH3:19])[CH:12]=1)[C:6]([O:8]C)=[O:7])(=O)C.Cl.[OH2:21]>CN1CCCC1=O>[Cl:18][C:14]1[C:15]([CH3:17])=[CH:16][C:11]([CH2:10][C:5](=[O:21])[C:6]([OH:8])=[O:7])=[CH:12][C:13]=1[CH3:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
29.4 g (105 mmol) methyl 2-acetylamino-3-(4-chloro-3,5-dimethylphenyl)-acrylate in 330 mL N-methyl-2-pyrrolidinone were combined with 500 mL cooled 4 M HCl, stirred for 6 h at reflux temperature and for 16 h at RT. After the reaction had ended the reaction mixture was poured onto 1650 mL water, stirred for 1 h, suction filtered and the crystals were dried at 50° C. in the vacuum drying cupboard. The product was recrystallised from toluene.
Workup
- temperatureat reflux temperature
- waitfor 16 h at RT
- stirringstirred for 1 h
- filtrationsuction filtered
- customthe crystals were dried at 50° C. in the vacuum
- customdrying cupboard
- customThe product was recrystallised from toluene
Sources & evidence
- ORD record
- ord-42df235181354a41b5b6874ca595717f
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696196B2
Reaction notes
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