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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897465Generated: October 26, 2026

Water → 5-Bromo-2-phenoxypyrimidine

https://huagongshe.com/reaction/897465

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 numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-ece28418e4614288bf5fd0fd7c32b5ee
Source noteuspto-grants-2005_07