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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398116Generated: November 1, 2026

Chloride → 3-Phenoxybenzaldehyde

https://huagongshe.com/reaction/2398116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
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 methalene 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 55 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. Yield (0.80 g.), b.p. 126°/0.8 mm.Hg, nD = 1.5984.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024163
Source datasetuspto-grants-1977_05
ORD IDord-d71c269b158d4cbc9e2f94fc7698466b
Source noteuspto-grants-1977_05