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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902898Generated: November 1, 2026

3-Phenoxybenzoic acid → 3-Phenoxybenzyl alcohol

https://huagongshe.com/reaction/1902898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenoxybenzoic acidHCID 19539—
Reactant3-PhenoxybenzaldehydeHCID 38284—
Product3-Phenoxybenzyl alcoholHCID 26295—

Reaction Steps

After filtering off the catalyst, the filtrate (reaction mixture), which consists of an organic phase containing the 3-phenoxy-benzaldehyde and an aqueous-alkaline phase containing the 3-phenoxy-benzoic acid is extracted with ether. After drying the combined ether extracts over sodium sulphate and stripping off the ether under nitrogen, 9.4 g of a residue which, according to analysis by gas chromatography, contains 96.9% of 3-phenoxy-benzaldehyde and 1.3% of still unreacted 3-phenoxy-benzyl alcohol remain. This gives a 3-phenoxy-benzyl alcohol conversion of 98.8%, a 3-phenoxy-benzaldehyde yield of 93% of theory and a selectivity for 3-phenoxy-benzaldehyde of 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04366325
Source datasetuspto-grants-1982_12
ORD IDord-1ac8ec003e9b4cc7bf650fc42b3aadcc
Source noteuspto-grants-1982_12