HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386549Generated: October 29, 2026
Diphenyl carbonate → Oxalic acid, diphenyl ester
https://huagongshe.com/reaction/1386549
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 triphenyl phosphine oxide and oxalyl chloride as catalysts, the mixture was heated to 90° C. and stirred for 1 hour. 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 10.3 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 2.0×10−6 mole, in terms of sodium, based on bisphenol A, to synthesize polycarbonate. The conditions and results are shown in Tables III-A and III-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-c08cdfe5f10740f9b73f3693ce1f096d |
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| Source note | uspto-grants-2001_07 |
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