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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038548Generated: October 31, 2026

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

https://huagongshe.com/reaction/2038548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chloro-5-methoxyphenyl)methanolHCID 12909342—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
Product3-Chloro-5-methoxybenzaldehydeHCID 2190463378%

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 (78%). 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 numberUS08575208B2
Source datasetuspto-grants-2013_11
ORD IDord-028a84b18aab4ce3a771fe6c2ed8443e
Source noteuspto-grants-2013_11