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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399192Generated: October 27, 2026

Ethanol → 2-(3-Benzyloxyphenyl)-5-bromopyrimidine

https://huagongshe.com/reaction/2399192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Benzyloxy-phenylboronic acidHCID 2734313—
Reactant2,5-DibromopyrimidineHCID 10955588—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(3-Benzyloxyphenyl)-5-bromopyrimidineHCID 1938622670.3%

Reaction Steps

15.00 g (63.10 mmol) of 2,5-dibromopyrimidine (for preparation see: D. W. Arantz and D. J. Brown in Journal of the Chemical Society C, 1971, p. 1889), 14.40 g (63.10 mmol) of 3-benzyloxybenzeneboronic acid, 13.40 g (126.2 mmol) of sodium carbonate and 0.73 g (0.63 mmol) of tetrakis(triphenylphosphine)palladium(0) are heated at 80° C. for 4 hours in 150 ml of toluene, 75 ml of ethanol and 50 ml of water. The reaction mixture is subsequently partitioned between ether and water, the organic phase is washed twice with sodium chloride solution, dried over sodium sulfate and evaporated, and the residue is purified by chromatography (silica gel/dichloromethane), giving 15.14 g of 5-bromo-2-(3-benzyloxyphenyl)pyrimidine. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05447656
Source datasetuspto-grants-1995_09
ORD IDord-72290be2f4eb48ca8a986b9580a1729a
Source noteuspto-grants-1995_09