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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508363Generated: November 3, 2026

Hydrochloric Acid → 4-bromo-1-(2-ethoxyethyl)-1H-pyrazole

https://huagongshe.com/reaction/1508363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl vinyl etherHCID 8023—
Reactant4-BromopyrazoleHCID 16375—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product4-bromo-1-(2-ethoxyethyl)-1H-pyrazoleHCID 51892139108.4%

Reaction Steps

To a solution of 4-bromopyrazole (70.0 g, 0.476 mol) in CH2Cl2 (600 mL) was added a solution of 3.1 M HCl in dioxane (4 mL) and ethyl vinyl ether (41 g, 0.569 mol, 1.2 equiv) at ambient temperature. The resulting reaction mixture was stirred at ambient temperature for 3 h. The reaction was quenched with aqueous NaHCO3 and the two layers were separated. The organic layer was washed with water, dried over Na2SO4, and concentrated under reduced pressure to dryness to afford 4-bromo-1-(ethoxyethyl)-1H-pyrazole (113 g, 104.3 g theoretical, 97% yield) as an oil (GC purity: 89%), which was directly used in the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221845B2
Source datasetuspto-grants-2015_12
ORD IDord-803d76ad4a584d1689df72f2d0548b04
Source noteuspto-grants-2015_12