Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358113Generated: October 28, 2026

Pyridine → 3-Phenoxybenzaldehyde

https://huagongshe.com/reaction/358113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
Catalystchromium (VI) trioxideHCID 10219390—
SolventDichloromethaneHCID 6344—
Product3-PhenoxybenzaldehydeHCID 38284—

Reaction Steps

Chromium trioxide (3.00 g.) was added to a stirred solution of pyridine (4.75 g.) in dry methylene chloride (75 ml.), and stirring was continued for a further 15 minutes. 3-Phenoxybenzyl alcohol (1 g.) in methylene chloride (5 ml.) was added, the mixture stirred for a further 15 minutes, decanted and the residue washed with diethyl ether (100 ml.). The filtrate was washed with 5% sodium hydroxide solution (3×50 ml), 2.5 NHCl (50 ml.) and 5% sodium carbonate solution (50 ml.) and dried over Na2SO4 to give 3-phenoxy-benzaldehyde. Alternatively the alcohol can be oxidized using Jones' reagent, a similar yield of aldehyde being obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464391
Source datasetuspto-grants-1984_08
ORD IDord-1e25c75842c54851b680058919429075
Source noteuspto-grants-1984_08