HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 18976205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18976182 | HCID 18976182 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18976205 | HCID 18976205 | 74.4% |
Reaction Steps
Under argon atmosphere, a mixture of 2.70 g of 3,4-dichloro-N-(2,3-dihydro-2-oxo-1-pentyl-1H-indol-3-yl)benzamide, 1.30 g of acrylonitrile, 30 ml of acetone and 1.46 g of potassium carbonate was stirred at room temperature for 1 hour. After removal of solvent, the residue was treated with water and extracted with ethyl acetate. After the ethyl acetate extract was washed and dried, the solvent was removed by evaporation. The residue was crystallized from ethyl acetate-hexane to afford 2.28 g of 3,4-dichloro-N-[3-(2-cyanoethyl)-2,3-dihydro-2-oxo-1-pentyl-1H-indol-3-yl]-benzamide as colorless crystals. Melting point: 79° to 84° C., IR (Nujol) (cm-1): 3340, 2325, 1700, 1655, 1610, MS (m/z): 445 & 443 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807883 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-9f49970edd1b4fcdb98718edfd1f1462 |
| Source note | uspto-grants-1998_09 |