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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897550Generated: October 31, 2026

4-Methoxybenzyl alcohol → 4-Methoxybenzaldehyde

https://huagongshe.com/reaction/1897550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantTriethylamineHCID 8471—
ReactantDiisopropylethylamineHCID 81531—
ReactantTempoHCID 2724126—
Solvent1,2-DichloroethaneHCID 11—
Product4-MethoxybenzaldehydeHCID 312445%

Reaction Steps

The effect of the additive was then examined for the oxidation of 4-methoxybenzylalcohol using 8 (2 mol %) in 1,2-dichloroethane (Table 2). Triethylamine, diisopropylethylamine, and TEMPO were all effective promoters of the vanadium complex, affording high yields of 4-methoxybenzaldehyde after 24 h at 60° C. (Entries 2 to 5). In contrast, less than 5% yield was observed with the vanadium complex alone (no additive, Entry 1), suggesting a key role for the nitrogen base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519132B2
Source datasetuspto-grants-2013_08
ORD IDord-bd5c66ef4f7246f08adbf502d6f29a3f
Source noteuspto-grants-2013_08