Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bromate | HCID 23668195 | — |
| Reactant | 2,3,5,6-Tetrabromo-4-[2-(4-hydroxyphenyl)propan-2-yl]phenol | HCID 54240982 | — |
| Reactant | HCID 131723160 | HCID 131723160 | — |
| Product | Bisphenol A | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06365786B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-4ee2d5f62d96463196ca04f6b806c260 |
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| Source note | uspto-grants-2002_04 |
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