Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57399Generated: October 30, 2026

Water → 1-(5-(4-Fluorophenoxy)pyrimidin-2-yl)ethanone

https://huagongshe.com/reaction/57399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(5-Fluoropyrimidin-2-yl)ethanoneHCID 50994815—
SolventDimethylformamideHCID 6228—
Product1-(5-(4-Fluorophenoxy)pyrimidin-2-yl)ethanoneHCID 8673017425.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 1-(5-fluoropyrimidin-2-yl)ethanone (700 mg, 5.0 mmol) and 4-fluorophenol (616 mg, 5.50 mmol) in 6 mL DMF was treated with potassium carbonate (829 mg 6.0 mmol) and heated to 50° C. for 3.5 h. The reaction mixture was poured into 20 mL water, and extracted with EtOAc (2×20 mL). Organics were washed with 20 mL each water, brine, and dried over Na2SO4. Mixture was filtered and concentrated on silica gel. Column chromatography (10-100% EtOAc/hept) gave 295 mg (25%) 1-(5-(4-fluorophenoxyl)pyrimidin-2-yl)ethanone as a white solid used directly in the following step. MS m/z 233.2 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 8.55 (s, 2H), 7.23-7.07 (m, 4H), 2.78 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-d0f2680d666849229155d96fe5e65953
Source noteuspto-grants-2016_09