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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565996Generated: October 29, 2026

(3-Methoxymethoxypyridin-2-yl)-(4-nitrophenyl)methanol → 2-(4-Aminobenzyl)-3-methoxymethoxypyridine

https://huagongshe.com/reaction/565996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Methoxymethoxypyridin-2-yl)-(4-nitrophenyl)methanolHCID 18472436—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(4-Aminobenzyl)-3-methoxymethoxypyridineHCID 1847220629.5%

Reaction Steps

A mixture of (3-methoxymethoxypyridin-2-yl)-(4-nitrophenyl)methanol (11.78 g) and 10% Pd—C (1.2 g) in ethanol (100 ml) was vigorously stirred under hydrogen atmosphere for 24 hours. The catalyst was filtered of, and the filtrate was concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:1→2:1) to give 2-(4-aminobenzyl)-3-methoxymethoxypyridine (2.92 g) as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-1681971700634f2ab13beb5a75a7402d
Source noteuspto-grants-2001_01