HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857031Generated: November 2, 2026
Bisphenol A → Carbonic acid;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol
https://huagongshe.com/reaction/1857031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Diphenyl carbonate | HCID 7597 | — |
| Product | Carbonic acid;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol | HCID 159987 | — |
Reaction Steps
A 1-l glass melt polymerization reactor was passivated by acid washing, rinsing with deionized water and overnight drying at 70° C. it was charged with 130.4 g (608.6 mmol) of diphenyl carbonate and 120 g (525.6 mmol) of bisphenol A. A solid nickel stirrer was suspended in the mixture and the reactor was purged with nitrogen and heated to 180° C., whereupon the reaction mixture melted. Upon complete melting, it was allowed to equilibrate for 5-10 minutes, with stirring. There were then added, with stirring, 600 μl of a 0.221 M aqueous tetramethylammonium maleate solution and 500 μl of a 0.01 M aqueous sodium hydroxide solution. Heating at 180° C. and stirring were continued for 5 minutes, after which the temperature was raised to 210° C. and the pressure decreased to 180 torr, whereupon phenol began to distill. After 10 minutes, a bisphenol A polycarbonate oligomer had been produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06143859 |
|---|
| Source dataset | uspto-grants-2000_11 |
|---|
| ORD ID | ord-9708b5af3119497bb2094e6ecd4b377e |
|---|
| Source note | uspto-grants-2000_11 |
|---|