Acetone → BPA phenol

HRID 634559Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 634559
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CC(C)=O.[OH:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]([C:22]2[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][CH:23]=2)([CH3:21])[CH3:20])=[CH:15][CH:14]=1>O>[OH:12][C:13]1[CH:14]=[CH:15][C:16]([C:19]([C:22]2[CH:23]=[CH:24][C:25]([OH:28])=[CH:26][CH:27]=2)([CH3:21])[CH3:20])=[CH:17][CH:18]=1.[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Komponenten

5

Edukt 3

HCID 180Acetone2×HCID 996Phenol2×HCID 6623Bisphenol A2×

Produkt 1

HCID 14618994BPA phenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Versuchsvorschrift

A process for producing a dihydric phenol preferably bisphenol-A consisting of the steps of (1) formulating reaction ingredients of phenol, acetone, recycle bisphenol A, impurities, an acid catalyst and water, (2) reacting the ingredients to form a product mix consisting of bisphenol-A, unreacted phenol, by-products, acetone and water, (3) crystallizing the product mix forming a slurry of bisphenol-A/phenol adduct crystals solid phase, (4) separating the solid phase from the liquid phase by filtration, (5) removing the phenol from the bisphenol-A/phenol adduct to obtain a crude bisphenol-A, and (6) purifying the crude bisphenol by fractional melt crystallization to obtain a bisphenol-A of at least 99.5% purity. Optionally, the process may include the steps of recycling the liquid phase from step (3) back to the reaction step after removal of the water of reaction, and further removing entrained phenol and acetone from the removed water of reaction which phenol and acetone is also recycled back to the reaction step.

Aufarbeitung

  1. customto form a product
  2. additionmix
  3. customcrystallizing the product
  4. additionmix

Quellen und Nachweise

ORD-Eintrag
ord-c5f7f274ee814d1fb824266f3f0bf02a
Quelldatensatz
uspto-grants-2001_02
Patentnummer
USH0001943H1

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