HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethenamine, N,N-dimethyl-2-nitro- → (E)-5-Chloro-2-ethyl-3-(2-nitroethenyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethenamine, N,N-dimethyl-2-nitro- | HCID 518458 | — |
| Reactant | 5-chloro-2-ethyl-1H-indole | HCID 20517175 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Diethylether ethylacetate | HCID 21584169 | — |
| Product | (E)-5-Chloro-2-ethyl-3-(2-nitroethenyl)-1H-indole | HCID 21974279 | — |
Reaction Steps
The indole 3 (5 mmol) was added to a stirred ice-cooled solution of 1-(dimethylamino)-2-nitroethylene (0.58 g, 5 mmol) in trifluoroacetic acid (5 mL). The mixture was stirred at room temperature under N2, for 0.5 h and then poured onto ice water. The aqueous solution was extracted with ethyl acetate, the combined organic layers were washed with a saturated NaHCO3 solution and then with water. After drying over Na2SO4, the solvent was evaporated under reduced pressure to give a crude orange solid which was suspended in a mixture of EtOAc-Et2O and filtered, or chromatographed on silica gel (cyclohexane/EtOAc, 1:1, as eluent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098233B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-fd5736776b90490195ef7a703ff54b79 |
| Source note | uspto-grants-2006_08 |