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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840407Generated: October 26, 2026

Hydrogen Bromide → Bisphenol A

https://huagongshe.com/reaction/840407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
ReactantSodium BromateHCID 23668195—
Reactant2,3,5,6-Tetrabromo-4-[2-(4-hydroxyphenyl)propan-2-yl]phenolHCID 54240982—
ReactantHCID 131723160HCID 131723160—
ProductBisphenol AHCID 6623—

Reaction Steps

A highly pure and colorless tetrabromobisphenol-A (TBBPA) possessing melting point in the range of 178-182° C. is prepared in yields of 50-70% in first batch and 90-100% when the spent organic layer is recycled. In this method, the corrosive liquid bromine is displaced by sodium bromide/hydrobromic acid as brominating agent. Further, sodium bromate is used as an oxidizing as well as brominating agent to utilize the hydrobromic acid that is produced during the bromination of bisphenol-A (BPA). The reaction is conducted at 10-15° C. in a mixture of methylene chloride-water or carbon tetrachloride-water in the presence of hydrochloric acid and sodium lauryl sulfate. The crystalline product settled at the bottom of the reaction vessel is filtered, washed, dried and weighed. The spent organic layer is recycled in subsequent batches to maximize the overall yield of product recovered directly as solid and to minimize generation of organic effluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365786B1
Source datasetuspto-grants-2002_04
ORD IDord-4ee2d5f62d96463196ca04f6b806c260
Source noteuspto-grants-2002_04