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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077611Generated: October 28, 2026

Phenol → Phenyl Salicylate

https://huagongshe.com/reaction/1077611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantDiphenyl carbonateHCID 7597—
ReactantCesium bromide (CsBr)HCID 24592—
ReactantHCID 21441352HCID 21441352—
ReactantHCID 178418416HCID 178418416—
CatalystPalladiumHCID 23938—
ProductPhenyl SalicylateHCID 8361—

Reaction Steps

3.0 g (32 mmol) of phenol, 25.8 mg (0.012 mmol Pd) of 5%-palladium/carbon, 4.2 mg (0.012 mmol) of cerium (III) acetate monohydrate, and 5.18 mg (0.24 mmol) of cesium bromide were charged in a 30-ml Hastelloy autoclave. After air in the system was replaced by carbon monoxide, 60 Kg/cm2 of carbon monoxide and 30 Kg/cm2 of dry air were introduced into the autoclave, followed by reaction at 100° C. for 3 hours. As a result of gas chromatographic analysis of the reaction solution, the yield of diphenyl carbonate was 9.4% (1.5 mmol). The yields of phenyl salicylate and p-phenoxyphenol which were produced as by-products were 0.32% (0.05 mmol) and 0.13% (0.02 mmol), respectively. After the completion of reaction, the gas phase contained 0.4% of carbon dioxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05543547
Source datasetuspto-grants-1996_08
ORD IDord-20b3fb0d27bf4ab2a44cf7416d9449ae
Source noteuspto-grants-1996_08