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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277171Generated: November 2, 2026

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

https://huagongshe.com/reaction/1277171

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 numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-b6027d1831e14029a090d80b2d8d510a
Source noteuspto-grants-2000_12