Reaction equation
C(O)(=O)C.C(N)CC.C([O-])(=O)C.C([NH3+])CC.[Cl:17][C:18]1[CH:19]=[C:20]([C:25]2[O:31][C:28]([CH:29]=O)=[CH:27][CH:26]=2)[CH:21]=[CH:22][C:23]=1[Cl:24].[N+:32]([CH3:35])([O-:34])=[O:33]>CO>[Cl:17][C:18]1[CH:19]=[C:20]([C:25]2[O:31][C:28](/[CH:29]=[CH:35]/[N+:32]([O-:34])=[O:33])=[CH:27][CH:26]=2)[CH:21]=[CH:22][C:23]=1[Cl:24]Participants
Conditions
- Temperature
- 0 °C
Procedure
A stirred solution of acetic acid (1.4 ml, 1.46 g, 24.3 mmol) in methanol (3.5 ml) under nitrogen atmosphere at 0° C. was treated dropwise with n-propylamine (2.0 ml, 1.42 g, 24.0 mmol). The resulting n-propylammonium acetate solution was stirred at 0° C. for 5 min, then added dropwise to a stirred solution of 5-(3,4-dichlorophenyl)furfural (10.04 g, 41.6 mmol) in nitromethane (6.8 ml, 7.61 g, 124.7 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 30 min. Then the cooling bath was removed, and stirring was continued at RT. From time to time, 10 ml of THF was added five times. After stirring overnight THF was evaporated and water was added. A solid was filtrated, washed with water and heptane to afford 11.46 g of 2-(3,4-dichlorophenyl)-5-((E)-2-nitrovinyl)furan. 1H NMR (400 MHz, DMSO-d6): 7.38 (1H, d), 7.43 (1H, d), 7.76 (1H, d), 7.95 (1H, dd), 8.03 (1H, d), 8.19 (1H, d), 8.31 (1H, d)
Workup
- customThen the cooling bath was removed
- stirringstirring
- customwas continued at RT
- additionFrom time to time, 10 ml of THF was added five times
- stirringAfter stirring overnight THF
- customwas evaporated
- additionwater was added
- filtrationA solid was filtrated
- washwashed with water and heptane
Sources & evidence
- ORD record
- ord-02b842f831f0463fb14cebfedd74b007
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975254B2
Linked notes
Loading…