HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Fenpiclonil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-Acetyl-4-(2,3-dichlorophenyl)-3-trifluoromethylpyrrole | HCID 21245533 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Fenpiclonil | HCID 91724 | — |
Reaction Steps
6.4 g of N-acetyl-4-(2,3-dichlorophenyl)-3-trifluoromethylpyrrole, 15 ml of 25% aqueous ammonia solution and 60 ml of dioxane are stirred for 18 hours at 160° C. in an autoclave. The reaction mixture is cooled to room temperature and filtered, and the clear filtrate is concentrated by evaporation. The viscous residue is dissolved in ethyl acetate; the solutiion is washed firstly with water and then with a diluted sodium chloride solution; it is subsequently dried over sodium sulfate, filtered, and concentrated by evaporation. To the residue is added n-hexane, and the crystals which precipitate are filtered off and dried. The yield is 5.3 g of 4-(2,3-dichlorophenyl)-3-cyanopyrrole, m.p. 149°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822919 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-61c863adc8624c1db47f39a7d6f04b12 |
| Source note | uspto-grants-1989_04 |