Propanamide, 2-chloro-N,N-dimethyl- → HCID 20370560, compound
Reaction equation
[CH3:1][C:2]1[C:3]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][NH:5][CH:6]=1.Br[CH:14]([CH2:20][CH3:21])[C:15]([N:17]([CH3:19])[CH3:18])=[O:16].[Cl:22]C(C)C(N(C)C)=O>>[Cl:22][C:12]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:3]1[C:2]([CH3:1])=[CH:6][N:5]([CH:14]([CH2:20][CH3:21])[C:15]([N:17]([CH3:19])[CH3:18])=[O:16])[N:4]=1Participants
4
Procedure
Following the procedure of Example 1, but substituting 3-(o-chlorophenyl)-4-methylpyrazole for 4-methyl-3-phenylpyrazole and 2-bromo-N,N-dimethylbutyramide for 2-chloro-N,N-dimethylpropionamide there was obtained 3-(o-chlorophenyl)-α-ethyl-N,N,4-trimethylpyrazole-1-acetamide having a boiling point of 180°/0.15 mm.
Sources & evidence
- ORD record
- ord-729db3861a994c868ed2724afee2840f