Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178469818HCID 178469818—
SolventWaterHCID 962—
ProductEthyl 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carboxylateHCID 2217507982%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-11786f95964a45ac9eeff59b3e79fee2
Source noteuspto-grants-2007_07