2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)- → HCID 54546950, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:16][CH3:17])[C:13]=1[O:14][CH3:15])[CH:6]=[CH:7][C:8](Cl)=[O:9].[CH2:18]([NH:24][C:25]([CH:27]([N:29]1[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]1)[CH3:28])=[O:26])[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:16][CH3:17])[C:13]=1[O:14][CH3:15])[CH:6]=[CH:7][C:8]([N:32]1[CH2:31][CH2:30][N:29]([CH:27]([C:25]([NH:24][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:26])[CH3:28])[CH2:34][CH2:33]1)=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6.39 g of 3,4,5-trimethoxycinnamoyl chloride is added with stirring at room temperature to a solution of 5.00 g of 1-[1-(hexylaminocarbonyl)ethyl]piperazine in 80 ml of chloroform, and the resulting solution is stirred at room temperature for 15 minutes.
Sources & evidence
- ORD record
- ord-b21d5d11324840fb9a0754e72a97ee67
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04478838
Reaction notes
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