HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386545Generated: October 31, 2026
Diphenyl carbonate → Oxalic acid, diphenyl ester
https://huagongshe.com/reaction/1386545
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphenyl carbonate | HCID 7597 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | Oxalic acid, diphenyl ester | HCID 18475 | — |
Reaction Steps
400 parts of an aqueous solution of sodium hydrogencarbonate having a pH of 10 were added to 200 parts of diphenyl carbonate, obtained through the decarbonylation reaction of diphenyl oxalate using tetraphenyl phosphonium bromide and hydrogen chloride as catalysts, and the mixture was heated to 90° C. and stirred for 1 hour. This washing step was repeated twice. To the obtained heavy solution (diphenyl carbonate layer) was further added 400 parts of distilled water, and the resulting mixture was heated to 90° C. and stirred for 1 hour to obtain diphenyl carbonate containing 1.5 ppm of hydrolyzable halogen. 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 2.0×10−6 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 II-A and II-B below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265524B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-8d7ffcb04fbd450a93f50d496118a202 |
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| Source note | uspto-grants-2001_07 |
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