HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → (E)-4-chloro-3-(2-nitrovinyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-Chloro-1H-indole-3-carboxaldehyde | HCID 13499089 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-4-chloro-3-(2-nitrovinyl)-1H-indole | HCID 21071472 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 4-chloroindole-3-carbaldehyde (314 mg, 1.75 mmol) and ammonium acetate (404 mg, 5.25 mmol) in nitromethane (6 mL) was stirred at 100° C. for 20 min. The reaction mixture was cooled, diluted with water and extracted with EtOAc (2×40 mL). The combined organic layers were washed with brine, dried over MgSO4 and concentrated under reduced pressure. The crude material was purified by silicagel column chromatography (50-100% EtOAc/heptane) to give compound B19-1 (224 mg, 58%) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365522B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-667568d9aac94626bb7287d0d56df59a |
| Source note | uspto-grants-2016_06 |