HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 21270102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 54724115 | HCID 54724115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21270102 | HCID 21270102 | 57% |
Reaction Steps
1.66 g of 2-[3-(N,N-dimethylamino)propylaminocarbonyl]-3-hydroxy-1-phenylindole hydrochloride are dissolved in 25 ml dichloromethane and mixed successively under vigorous agitation with 0.6 ml of triethylamine and 0.3 ml of acetyl chloride. The reaction mixture is boiled for 30 min under reflux. After cooling, the mixture is washed with a small amount of a saturated solution of sodium chloride, the organic phase dried over sodium sulfate and evaporated under vacuum. Following recrystallization from isopropanol, 1.00 g (57% of theoretical) 2[3-(N,N-diethylamino)-propylaminocarbonyl]-3-acetoxy-1-phenylindole hydrochloride is obtained. Melting point: 174°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814345 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-0c5fa10195fa4972879b9f20f9ba0006 |
| Source note | uspto-grants-1989_03 |