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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Benzyloxy-phenylboronic acid | HCID 2734314 | — |
| Reactant | 2,5-Dibromopyrimidine | HCID 10955588 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-2-[4-(phenylmethoxy)phenyl]pyrimidine | HCID 564028 | 100.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05550236 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-7522b677a89d4482841967e4c53bf8fc |
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| Source note | uspto-grants-1996_08 |
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