HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382491Generated: October 30, 2026
Acetyl chloride → HCID 86584269, compound
https://huagongshe.com/reaction/382491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 86593055 | HCID 86593055 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86584269 | HCID 86584269 | — |
Reaction Steps
Under an inert atmosphere, acetyl chloride (29.1 ml, 0.385 mol) is slowly added to a suspension of aluminum chloride (51.2 g, 0.385 mol) stirred in 1,2-dichloroethane (750 ml). After stirring at room temperature for 1 hour a yellow solution is obtained. The solution is cooled in an ice bath and N,N-dimethyl-2-(2′,3′,5′,6′-tetrafluoroanilino)phenylacetamide (40 g, 0.123 mol) is added. The reaction is allowed to warm to room temperature and then warmed to 80° for 0.5 hours. The reaction is poured over ice and extracted with EtOAc (2×750 ml). The organic extract is washed with water (750 ml), saturated NaHCO3 solution (500 ml) and brine (500 ml). Evaporation on a rotovap and trituration with Et2O gives N,N-dimethyl-5-acetyl-2-(2′,3′,5′,6′-tetrafluoroanilino)phenylacetamide as a white solid, m.p. 112-114°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06310099B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-f3a29fc9dbb74d9e9346fda466dc306d |
|---|
| Source note | uspto-grants-2001_10 |
|---|