HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295219Generated: October 27, 2026
Dimethylformamide → Ethyl 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carboxylate
https://huagongshe.com/reaction/1295219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178469818 | HCID 178469818 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carboxylate | HCID 22175079 | 82% |
Reaction Steps
A mixture of ethyl 3-hydroxy-1-methyl-1H-pyrazole-4-carboxylate (25.50 g), benzyl bromide (17.8 ml), potassium carbonate (31.10 g) and N,N-dimethylformamide (250 ml) was stirred overnight at 50° C. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dilute hydrochloric acid, washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and ethyl 3-benzyloxy-1-methyl-1H-pyrazole-4-carboxylate (31.90 g, yield 82%) was obtained as a colorless crystal from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio) and recrystallized from ethyl acetate-hexane. melting point: 66–67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07241785B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-11786f95964a45ac9eeff59b3e79fee2 |
|---|
| Source note | uspto-grants-2007_07 |
|---|