HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386539Generated: October 29, 2026
Diphenyl carbonate → Oxalic acid, diphenyl ester
https://huagongshe.com/reaction/1386539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl carbonate | HCID 7597 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Catalyst | Tetraphenylphosphonium Chloride | HCID 164911 | — |
| Solvent | Water | HCID 962 | — |
| Product | Oxalic acid, diphenyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06265524B1 |
|---|
| Source dataset | uspto-grants-2001_07 |
|---|
| ORD ID | ord-94e1487809514e4ca815d187abc6e104 |
|---|
| Source note | uspto-grants-2001_07 |
|---|