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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861676Generated: October 29, 2026

Phenyl benzoate → Methyl Benzoate

https://huagongshe.com/reaction/861676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl benzoateHCID 7169—
ReactantDiphenyl carbonateHCID 7597—
ReactantDimethyl CarbonateHCID 12021—
ReactantCarbonic acid, methyl phenyl esterHCID 139482—
CatalystTitanium tetra(phenolate)HCID 6451468—
ProductMethyl BenzoateHCID 7150—
ProductPhenyl benzoateHCID 7169—

Reaction Steps

Phenyl benzoate was synthesized using the same method as in Example 9. Next, into an autoclave made of SUS316 having an internal volume of 100 ml were charged the synthesized phenyl benzoate 30 g (151 mmole), dimethyl carbonate 6.82 g (75.7 mmole) and titanium tetraphenoxide 0.02 g (0.045 mmole). After replacing the air with nitrogen, the autoclave was sealed and the contents were reacted for two hours at 200° C. After completing the reaction, the reaction mixture was analyzed by gas chromatography. As a result, the yield of methyl phenyl carbonate was 15%, and the yield of diphenyl carbonate was 4%. Furthermore, at the same time, methyl benzoate was produced as a by-product with a yield of 19% (the yield is given in terms of phenyl benzoate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714627
Source datasetuspto-grants-1998_02
ORD IDord-02d92e4c7e2347a6933ee5d6a97eea61
Source noteuspto-grants-1998_02