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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654826Generated: November 1, 2026

2-Amino-3-Hydroxypyridine → 3-[(4-Methoxybenzyl)oxy]pyridin-2-amine

https://huagongshe.com/reaction/1654826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-HydroxypyridineHCID 28114—
Reactant4-Methoxybenzyl bromideHCID 165021—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product3-[(4-Methoxybenzyl)oxy]pyridin-2-amineHCID 272838976.7%

Reaction Steps

A mixture of 4-methoxybenzyl bromide (25 g, 0.159 mol) and 2-amino-3-hydroxypyridine (15.9 g, 0.145 mol) in 40% aqueous sodium hydroxide solution (150 ml) and dichloromethane (150 ml) was treated with Adogen 464 (5 ml) and stirred vigorously at room temperature for 16 hours. The mixture was diluted with further water and dichloromethane, the product extracted into dichloromethane, and the combined organic layers washed with water, dried and evaporated. The resulting solid was washed with ether to yield the product (25.6 g, 70%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409943
Source datasetuspto-grants-1995_04
ORD IDord-c45126958ef04d6a85f2ce607e71d9cf
Source noteuspto-grants-1995_04