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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228186Generated: October 28, 2026

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

https://huagongshe.com/reaction/2228186

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 numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-0c578bfd9bb04612b4a50377a26f0a62
Source noteuspto-grants-2002_07