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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811367Generated: October 30, 2026

Potassium Carbonate → HCID 178419375, compound

https://huagongshe.com/reaction/1811367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantHCID 178473861HCID 178473861—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 178419375HCID 178419375—

Reaction Steps

A suspension of 1-acetyl-3-hydroxy-pyrazole (1.0 g, 7.9 mmol), 2-bromobenzyl bromide (2.0 g, 7.9 mmol) and K2CO3 (1.2 g, 8.4 mmol) in 20 mL of 2-butanone was heated to reflux for 90 min. After cooling to room temperature, the precipitated salts were filtered off and rinsed with tert-butyl methyl ether (TBME). The filtrate was then concentrated under reduced pressure (50 mbar) and redissolved in a mixture of tetrahydrofuran (THF) and methanol (MeOH) (3:2, 25 mL). 1 mL of a 10% NaOH solution was added and the solution was stirred 60 min at ambient temperature. Then, all volatiles were removed under reduced pressure (50 mL). The residue was diluted with 10 mL of H2O and 20 mL of ethyl acetate (EtOAc). The aqueous phase was extracted with EtOAc (2×10 mL). The combined organic layers were washed with water and brine (both 20 mL) and dried over Na2SO4. The crude product was obtained after evaporation of all volatiles and used in the next step without further purification (1.9 g, 7.5 mmol, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362271B2
Source datasetuspto-grants-2013_01
ORD IDord-10fe0c12567e44fa80c8eeaad4330520
Source noteuspto-grants-2013_01