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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078799Generated: October 30, 2026

Ethanol → 5-Bromo-2-[4-(phenylmethoxy)phenyl]pyrimidine

https://huagongshe.com/reaction/1078799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-Benzyloxy-phenylboronic acidHCID 2734314—
Reactant2,5-DibromopyrimidineHCID 10955588—
CatalystTriphenylphosphineHCID 11776—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Bromo-2-[4-(phenylmethoxy)phenyl]pyrimidineHCID 564028100.4%

Reaction Steps

104.25 g (0.438 mol) of 2,5-dibromopyrimidine, 100.00 g (0.438 mol) of 4-(phenylmethoxy)benzeneboronic acid, 4.75 g (0.00438 mol) of palladium (10%) on activated carbon, 4.50 g (0.01752 mol) of triphenylphosphine and 93.00 g (0.876 mol) of sodium carbonate are heated in 1000 ml of toluene, 500 ml of ethanol and 300 ml of water for 24 hours at 80° C. The palladium catalyst is subsequently separated off from the reaction mixture at 80° C. by filtration. The aqueous lower phase of the reaction mixture is separated off at 80° C., before the organic phase is freed of the solvents on a rotary evaporator and dried in a high vacuum. The crude product thus obtained is recrystallized from acetonitrile (3000 ml), giving 150.07 g (97% yield, based on 2,5-dibromopyridine) of 5-bromo-2-[4-(phenylmethoxy)phenyl]pyrimidine (purity according to HPLC: 98%). ##STR4## mp.: 153°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550236
Source datasetuspto-grants-1996_08
ORD IDord-7522b677a89d4482841967e4c53bf8fc
Source noteuspto-grants-1996_08