HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → Fluquazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-[N-(2,2,2-trifluoroethyl)-trichloroacetamido]-5-chlorobenzophenone | HCID 12427480 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Fluquazone | HCID 219069 | — |
Reaction Steps
To a solution of 2.8 g of 2-[N-(2,2,2-trifluoroethyl)-trichloroacetamido]-5-chlorobenzophenone in 50 ml. of ethanol was added 4.6 g of ammonium acetate. The mixture was stirred and heated under reflux for 10 hours. Then the solvent was removed under reduced pressure. The residue was triturated with ether, filtered, washed with water and dried to give 1-(2,2,2-trifluoroethyl)-4-phenyl-6-chloro-2(1H)-quinazolinone. Recrystallization from ethanol gave pale yellow crystals, m.p. 185.0°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04202895 |
| Source dataset | uspto-grants-1980_05 |
| ORD ID | ord-a61302b74f264adcb990dd3b9c1fc28b |
| Source note | uspto-grants-1980_05 |