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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109724Generated: October 30, 2026

Benzyl Alcohol → 2-Benzyloxy-6-bromopyridine

https://huagongshe.com/reaction/1109724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant2,6-DibromopyridineHCID 12274—
Product2-Benzyloxy-6-bromopyridineHCID 81747576%

Reaction Steps

2,6-Dibromopyridine was condensed with benzyl alcohol by Ullmann reaction to obtain 2-benzyloxy-6-bromopyridine (yield 76%). This was further condensed with m-cresol by Ullmann reaction to obtain 2-benzyloxy-6-(3-methylphenoxy)-pyridine (yield 83%), which was then subjected to catalytic reduction in the presence of a catalyst, 5% palladium-carbon, to obtain 6-(3-methylphenoxy)-2-pyridone (yield 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322845
Source datasetuspto-grants-1994_06
ORD IDord-51cb2f199786405ca003de1b23808b24
Source noteuspto-grants-1994_06