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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274750Generated: October 25, 2026

Benzyl Bromide → ethyl 1-benzyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/274750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
SolventDimethylformamideHCID 6228—
Productethyl 1-benzyl-1H-pyrazole-4-carboxylateHCID 15237993—

Reaction Steps

To a suspension of sodium hydride (containing 63%, 652 mg) in dimethylformamide (abbreviated as DMF hereinafter) was added a solution of 4-ethoxycarbonylpyrazole (2.00 g) in DMF (15 ml) at room temperature. After stirred for 30 min at room temperature, to the mixture was added benzylbromide (2.04 ml). After stirred for 30 min, the mixture was quenched by addition of water. The mixture was extracted with ethyl acetate-n-hexane. The extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and evaporated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to give the title compound (2.98 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389666
Source datasetuspto-grants-1995_02
ORD IDord-da84e581f053455c945e01a9620ca8ee
Source noteuspto-grants-1995_02