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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246603Generated: November 3, 2026

2-Hydroxy-5-nitrobenzyl alcohol → (2-Methoxy-5-nitrophenyl)methanol

https://huagongshe.com/reaction/1246603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-5-nitrobenzyl alcoholHCID 2763823—
Reactant2-Methoxy-5-nitrobenzaldehyde methyl hemiacetalHCID 21014460—
Product(2-Methoxy-5-nitrophenyl)methanolHCID 1760424176%

Reaction Steps

This compound was prepared by reduction of 2-methoxy-5-nitrobenzaldehyde methyl hemiacetal using a method similar to that described for preparing 2-hydroxymethyl-4-nitrophenol in 76% yield: MP 121–122° C.; 1H NMR (DMSO-d6, 500 MHz) δ8.22 (d, 1H, J=1.22 Hz), 8.16 (dd, 1H, J=2.7 and 9.1), 7.16 (d, 1H, J=8.9 Hz), 4.50 (s, 2H), 3.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129225B2
Source datasetuspto-grants-2006_10
ORD IDord-0ad0a31cd04940c588c1c7f04550527d
Source noteuspto-grants-2006_10