HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1-(2-Fluoro-4-chloro-5-allyloxyphenyl)-3,4,5-trimethylpyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazole | HCID 13798233 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2-Fluoro-4-chloro-5-allyloxyphenyl)-3,4,5-trimethylpyrazole | HCID 13798273 | 97.3% |
Reaction Steps
A mixture of 1-(2-fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazole (25.5 g), allyl bromide (13.3 g), anhydrous potassium carbonate (14.5 g) and acetonitrile (150 ml) was heated under reflux, with stirring for 3 hours. After cooling, the reaction mixture was filtered through a filter to remove the inorganic salts therefrom and the filtrate was concentrated to a small volume under reduced pressure, affording the titled compound (28.7 g) as a pale brown crystalline solid. Recrystallization of this solid from cyclohexane yielded a white crystalline solid. m.p. 97°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04752326 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-1d1d2e107bcd4aa8bc568ea5c96b3a86 |
| Source note | uspto-grants-1988_06 |