HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(2,4-Dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178481842 | HCID 178481842 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-(2,4-Dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole | HCID 13321713 | 93% |
Reaction Steps
To a mixture of 1.50 g (0.0055 mol) of 4-(2,4-dichlorobenzoyl)-1-methyl-5-hydroxypyrazole, 0.56 g (0.0055 mol) of triethylamine and 30 ml of benzene was added 1.03 g (0.0061 mol) of benzyl bromide and the resulting mixture was heated under reflux for 2 hours with stirring. After cooling, precipitated triethyl amine hydrobromide was filtered off. The filtrate was concentrated under reduced pressure and was subjected to column chromatography (silica gel, using ethyl acetate/benzene 1:3 as an eluent) to give 1.79 g of the title compound 4-(2,4-dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole (yield: 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04557753 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-93814bf7ece5461c8ceb234868deca12 |
| Source note | uspto-grants-1985_12 |