Reaktion #927589

ord-4ee2d5f62d96463196ca04f6b806c260

Reaktionsgleichung

[Na+].[O-][Br+2]([O-])[O-]
sodium bromate
CC(C)(c1ccc(O)cc1)c1c(Br)c(Br)c(O)c(Br)c1Br
tetrabromobisphenol-A
BrBr
bromine
Br
hydrobromic acid
Br.[Br-].[Na+]
sodium bromide hydrobromic acid
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
bisphenol-A

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigein the range of 178-182° C.
  2. 2
    Sonstigeis prepared
  3. 3
    Sonstigein yields of 50-70% in first batch and 90-100% when the spent organic layer

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06365786B1uspto-grants-2002_04