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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654578Generated: November 3, 2026

Bromide ion → Diphenyl carbonate

https://huagongshe.com/reaction/654578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantCarbon DioxideHCID 280—
ReactantOxygenHCID 977—
ReactantPhenolHCID 996—
ReactantQuinoneHCID 4650—
ReactantDiphenyl EtherHCID 7583—
ReactantHCID 178418416HCID 178418416—
CatalystCobalt diacetateHCID 6277—
Catalystpalladium(II) acetateHCID 167845—
ProductDiphenyl carbonateHCID 759722%

Reaction Conditions

Temperature100 °C

Reaction Steps

Procedure of Example 1 was repeated except there was utilized 50.1 grams of phenol, 6.281 grams of diphenyl ether, 1.955 grams of benzoquinone, 1.5 gram of tetraabutylammonium bromide, 0.060 of palladium (II) acetate and 0.032 gram of cobalt (II) acetate. The reactor was sealed and pressurized with 400 psi of oxygen, 450 psi of carbon dioxide, and 800 psi of carbon monoxide to provide a total pressure of 1650 psi at room temperature. The reactor was heated to 100° C. At 0.5 hours, the pressure of the reactor was reduced to 1200 psi and then repressurized with 400 psi of oxygen and 600 psi of carbon monoxide. After 1 hour, the pressure of the reactor was reduced to 1000 psi, then repressurized with 350 psi of oxygen and 700 psi of carbon monoxide. The aforementioned repressurizing procedure was repeated after 2 hours had elapsed. At this time, a sample of the reaction mixture showed that it contained 22% yield of diphenyl carbonate based on GC. After the reaction had been running for 5 hours the mixture showed that it contained 14.85 grams or a 26.1% yield of diphenyl carbonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132447
Source datasetuspto-grants-1992_07
ORD IDord-0057dbd5d466430c8e089d9f49fd2586
Source noteuspto-grants-1992_07