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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581191Generated: November 1, 2026

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

https://huagongshe.com/reaction/581191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Benzyloxy-phenylboronic acidHCID 2734314—
ReactantTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
Reactant2,5-DibromopyrimidineHCID 10955588—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Bromo-2-[4-(phenylmethoxy)phenyl]pyrimidineHCID 56402897.9%

Reaction Steps

10.43 g (0.044 mol) of 2,5-dibromopyrimidine, 10 g (0.044 mol) of 4-(phenylmethoxy)benzeneboronic acid, 253 mg (0.00044 mol) of Pd(dba)2, (0.001752 mol) of TPPTS and 9.3 g (0.0876 mol) of sodium carbonate are heated at 80° C. in 100 ml of toluene, 50 ml of ethanol and 30 ml of water for 48 hours. The palladium catalyst is subsequently separated at 80° C. from the reaction mixture by filtration. The lower aqueous 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 is dried in a high vacuum. The crude product thus obtained is crystallized from acetonitrile (300 ml), giving 14.7 g (93% yield, based on 2,5-dibromopyrimidine) of 5-bromo-2-[4-(phenylmethoxy) phenyl]pyrimidine (content according to HPLC: 98%). ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919930
Source datasetuspto-grants-1999_07
ORD IDord-506a1447985f462fa33792834e4dd072
Source noteuspto-grants-1999_07