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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863581Generated: October 30, 2026

2-Phenoxybenzoic acid → o-Phenoxybenzaldehyde

https://huagongshe.com/reaction/863581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenoxybenzoic acidHCID 75237—
ReactantCornforth reagentHCID 2724130—
Reactant2-Phenoxybenzyl alcoholHCID 3660111—
Reactantlithium aluminium hydride THFHCID 68718528—
SolventDichloromethaneHCID 6344—
Producto-PhenoxybenzaldehydeHCID 8806078%

Reaction Steps

A mixture of 2-phenoxybenzyl alcohol (4.0 g, 20.2 mmol, prepared by the reduction of commercially available 2-phenoxybenzoic acid with LiAlH4 /THF) and 150 mL CH2Cl2 was treated with pyridinium dichromate (11.39 g, 30.3 mmol) at 25° C. and stirred for another 36 hours. The mixture was filtered through d.e. and then through a pad of silica gel to produce 3.11 g (78%) of title compound as a yellow oil. 1H NMR (CDCl3) δ6.8 (d, 1H), 6.9 (d, 1H), 7.0 (m, 2H), 7.1 (m, 2H), 7.2 (m, 1H), 8.9 (m, 1H), 10.2 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721255
Source datasetuspto-grants-1998_02
ORD IDord-404ef53e5420495e896d2796b7bf052d
Source noteuspto-grants-1998_02