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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526401Generated: October 30, 2026

Ethyl bromoacetate → ethyl 2-(4-cyano-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/526401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Pyrazole-4-carbonitrileHCID 564449—
SolventAcetoneHCID 180—
SolventHeptaneHCID 8900—
Productethyl 2-(4-cyano-1H-pyrazol-1-yl)acetateHCID 11760022651.9%

Reaction Steps

Combined 1H-pyrazole-4-carbonitrile (0.432 g, 4.64 mmol) in acetone (9.28 mL), potassium carbonate (1.924 g, 13.92 mmol) and ethyl 2-bromoacetate (1.027 mL, 9.28 mmol). The reaction mixture was stirred at room temperature overnight, then concentrated in vacuo, diluted with EtOAc (10 mL), washed with water (10 mL), dried (MgSO4) and concentrated in vacuo to give a residue. The residue was purified using flash column chromatography on silica gel (EtOAc in heptane, 10-50% gradient) to give a white solid. The solid was suspended in heptane and then filtered and dried to give the title compound (0.4314 g, 51.9% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21 (t, J=7.20 Hz, 3H) 4.17 (q, J=7.07 Hz, 2H) 5.19 (s, 2H) 8.11 (s, 1H) 8.57 (s, 1H). MS m/z [M+H]+ 180.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-5ab0affdf85f48a191238daf0f0634c6
Source noteuspto-grants-2016_05