1,2-Dichloroethane → HCID 53740612, compound
Reaction equation
[CH2:1]([NH2:9])[CH2:2][CH:3]=[CH:4][CH2:5][CH2:6][CH2:7][NH2:8].[CH2:10](Cl)[CH2:11]Cl.[C:14](=[O:17])([O-])[O-].[K+].[K+].[CH3:20][O:21][C:22]1[CH:30]=[CH:29][C:25]([C:26](Cl)=[O:27])=[CH:24][CH:23]=1>O>[CH2:1]([NH:9][C:14](=[O:17])[C:11]1[CH:10]=[CH:30][C:22]([O:21][CH3:20])=[CH:23][CH:24]=1)[CH2:2][CH:3]=[CH:4][CH2:5][CH2:6][CH2:7][NH:8][C:26](=[O:27])[C:25]1[CH:29]=[CH:30][C:22]([O:21][CH3:20])=[CH:23][CH:24]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
m.p. 141°-143° C., 10.2 g., was prepared as in Example 21 using 8.37 g. of 3-heptene-1,7-diamine, 50 ml. of ethylene dichloride, 18.0 g. of potassium carbonate, 100 ml. of water, 22.4 g. of 4-methoxybenzoyl chloride in 50 ml. ethylene dichloride and recrystallization from methanol.
Workup
- custom, was prepared as in Example 21 using 8.37 g
- customethylene dichloride and recrystallization from methanol
Sources & evidence
- ORD record
- ord-37cddb9afff44fe0866106b8d0f35054
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04009208
Reaction notes
Loading…