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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386539Generated: October 29, 2026

Diphenyl carbonate → Oxalic acid, diphenyl ester

https://huagongshe.com/reaction/1386539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl carbonateHCID 7597—
CatalystHydrochloric AcidHCID 313—
CatalystTetraphenylphosphonium ChlorideHCID 164911—
SolventWaterHCID 962—
ProductOxalic acid, diphenyl esterHCID 18475—

Reaction Steps

400 parts of distilled water were added to 200 parts of diphenyl carbonate, obtained through the decarbonylation reaction of diphenyl oxalate using a hydrochloride of tetraphenyl phosphonium chloride as a catalyst, and the mixture was heated to 90° C. and stirred for 1 hour to obtain diphenyl carbonate containing 5.8 ppm of hydrolyzable chlorine. An ester interchange reaction between this diphenyl carbonate and bisphenol A was carried out in the same manner as in Example 1 except that a disodium salt of bisphenol A was used in place of sodium hydroxide as an ester interchange catalyst in an amount of 3.5×10−5 mole, in terms of sodium, based on bisphenol A, to synthesize polycarbonate. A pellet of this polycarbonate was used for the measurement of its physical properties. The conditions and results are shown in Tables I-A and I-B below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265524B1
Source datasetuspto-grants-2001_07
ORD IDord-94e1487809514e4ca815d187abc6e104
Source noteuspto-grants-2001_07