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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432175Generated: October 26, 2026

Water → 5-Bromo-2-phenoxypyrimidine

https://huagongshe.com/reaction/432175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenolHCID 996—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
CatalystDibenzo-18-crown-6HCID 26541—
SolventTolueneHCID 1140—
Product5-Bromo-2-phenoxypyrimidineHCID 64284254.4%

Reaction Steps

A mixture of 5-bromo-2-chloropyrimidine (5.00 g, 0.0259 mol), phenol (3.16 g, 0.0336 mol), dibenzo-18-crown-6 (0.47 g, 0.0013 mol) and ground potassium hydroxide (3.51 g, 0.0626 mol) in toluene (75 ml) was heated at reflux for 5 hours with azeotropic removal of water. The mixture was allowed to cool to ambient temperature and the solvent was removed under reduced pressure. The residue was partitioned between water and chloroform. The layers were separated and the aqueous phase was extracted with chloroform three times. The combined organic layers were dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography on silica using n-heptane/ethyl acetate (98:2) as an eluent to give 5-bromo-2-phenoxy-pyrimidine as a white solid (3.55 g, 0.0141 mol): 1H NMR (DMSO-d6, 400 MHz) 8.80 (s, 2H), 7.45 (t, 2H), 7.27 (t, 1H), 7.22 (d 2H); TLC (n-heptane/ethyl acetate=95:5) Rf 0.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-1bbc8bd3d0a34185a80347e464788c0c
Source noteuspto-grants-2003_12