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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357897Generated: October 30, 2026

Phenethyl bromide → 1-(2-Phenylethyl)-3-amino-4-ethoxycarbonylpyrazole

https://huagongshe.com/reaction/357897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178469928HCID 178469928—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventTolueneHCID 1140—
Product1-(2-Phenylethyl)-3-amino-4-ethoxycarbonylpyrazoleHCID 2210382964.6%

Reaction Steps

250 ml of toluene and 0.1 ml of aqueous 12.5M sodium hydroxide solution were added to a mixture of 15.69 g of ethyl 3-amino-4-pyrazolecarboxylate, 24.34 g of (2-bromoethyl)benzene, 2.54 g of Adogen 464 and 27.74 g of potassium carbonate, and heated under reflux for 2.5 hours. The reaction solution was washed with 200 ml of water and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography (n-hexane-ethyl acetate=2:1→1:1→1:2) to obtain 16.94 g of 1-(2-phenylethyl)-3-amino-4-ethoxycarbonylpyrazole as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840909
Source datasetuspto-grants-1998_11
ORD IDord-af901bc0790f4cba99e350b7d30c22f3
Source noteuspto-grants-1998_11