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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425292Generated: October 28, 2026

(3-Chloro-5-methoxyphenyl)methanol → 3-Chloro-5-methoxybenzaldehyde

https://huagongshe.com/reaction/2425292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chloro-5-methoxyphenyl)methanolHCID 12909342—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
Product3-Chloro-5-methoxybenzaldehydeHCID 2190463377.1%

Reaction Steps

A mixture of 3-chloro-5-methoxybenzyl alcohol (5.0 g, 28.9 mmol) and pyridinium chlorochromate (20% on alumina, 40 g, 37.8 mmol) was allowed to stir for 1.25 hr. Diethyl ether (200 ml) was then added followed by filtration of precipitate. The filtrate was concentrated under reduced pressure and the resulting residue was purified via silica gel chromatography using 40% dichloromethane, 60% petroleum ether as eluant, to give 3.8 g of 3-chloro-5-methoxybenzaldehyde. 1H-NMR (CDCl3): 3.84 (s, 3H) 7.13 (s, 1H), 7.28 (s, 1H), 7.41 (s, 1H), 9.89 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964624B1
Source datasetuspto-grants-2011_06
ORD IDord-aec195a34ddc49a8a6268efc4cacbe85
Source noteuspto-grants-2011_06