HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(2,4-Dichlorobenzoyl)-1-methyl-5-(2-chlorobenzyloxy)-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | o-Chlorobenzyl methanesulfonate | HCID 20255346 | — |
| Reactant | HCID 178481842 | HCID 178481842 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(2,4-Dichlorobenzoyl)-1-methyl-5-(2-chlorobenzyloxy)-pyrazole | HCID 13321716 | 77.4% |
Reaction Steps
To a mixture of 1.33 g (0.0049 mol) of 4-(2,4-dichlorobenzoyl)-1-methyl-5-hydroxypyrazole, 0.54 g (0.0054 mol) of triethylamine and 30 ml of toluene was added 1.3 g (0.0059 mol) of o-chlorobenzyl methanesulfonate. Then, the reaction mixture was refluxed with stirring for 2 hours. After cooling, the reaction mixture was washed with 20 ml of water three times, and the organic layer was separated. After drying over anhydrous sodium sulfate, the organic layer was concentrated under reduced pressure and was subjected to a column chromatography (silica gel, eluent; ethyl acetate:benzene=1:9) to obtain 1.5 g of the title compound (yield: 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04557753 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-43f42231fe0c4fca82740b131934f7da |
| Source note | uspto-grants-1985_12 |