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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175288Generated: October 29, 2026

Potassium Carbonate → 2-(3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenoxy)ethyl acetate

https://huagongshe.com/reaction/2175288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
Reactant3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenolHCID 70982914—
SolventDimethylformamideHCID 6228—
Product2-(3-((4-Bromo-1H-pyrazol-1-yl)methyl)phenoxy)ethyl acetateHCID 7098281334%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 3-((4-bromo-1H-pyrazol-1-yl)methyl)phenol (0.6 g, 2.37 mmol), 2-bromoethyl acetate (0.792 g, 4.74 mmol) and potassium carbonate (0.655 g, 4.74 mmol) in DMF (5 mL) was heated at 200° C. in a microwave reactor for 1 h. After this time, the reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated. The resulting residue was purified by flash chromatography (0-100% ethyl acetate:hexanes) to afford the title compound (0.27 g, 34% yield) as a colorless oil. LCMS, [M+H]+=339.0. 1H NMR (400 MHz, CDCl3) δ 7.46 (s, 1H), 7.34 (s, 1H), 7.24 (dd, J=8.3, 7.6 Hz, 2H), 6.83 (dd, J=8.3, 2.4 Hz, 1H), 6.80 (d, J=7.6 Hz, 1H), 6.74 (d, J=2.4 Hz, 1H), 5.20 (s, 2H), 4.41-4.32 (m, 2H), 4.14-4.08 (m, 2H), 2.06 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062028B2
Source datasetuspto-grants-2015_06
ORD IDord-ca5dc099bc244b0b8a59fb1957e7d919
Source noteuspto-grants-2015_06