Formaldehyde → 2-Tert-Butylphenol

HRID 223279

Reaktionsgleichung

Reaktionsgleichung von HRID 223279
O[C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:11]2C=CC(O)=CC=2)([CH3:10])[CH3:9])=[CH:4][CH:3]=1.C1C=C(CC2C([OH:31])=CC=CC=2)C(O)=CC=1.C=O.C1C(C(C2C=CC(O)=CC=2)=C(Cl)Cl)=CC=C(O)C=1.C1(=O)CCCCC1.C1(O)C=CC=CC=1>CC(C)=O>[C:8]([C:5]1[CH:6]=[CH:7][CH:2]=[CH:3][C:4]=1[OH:31])([CH3:11])([CH3:10])[CH3:9]

Komponenten

8

Edukt 6

HCID 712FormaldehydeHCID 996PhenolHCID 6623Bisphenol AHCID 7967CyclohexanoneHCID 75575Bis(2-hydroxyphenyl)methaneHCID 846771,1-Bis(4-hydroxyphenyl)-2,2-dichloroethylene

Produkt 1

HCID 69232-Tert-Butylphenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel2×

Versuchsvorschrift

Bisphenols are exemplified by Bisphenol A, Bisphenol F, Bisphenol C, Bisphenol H and the like. As is well known, Bisphenol A is a dihydric phenol obtained by condensation of phenol and acetone, that is, 2,2-bis(4-hydroxyphenyl)propane; Bisphenol F is the corresponding compound obtained by using formaldehyde instead of the above mentioned acetone; Bisphenol C is the compound obtained by using cyclohexanone instead of the acetone; and Bisphenol H is a dihydric phenol obtained by condensation of o-tert-butyl phenol and acetone. These bisphenols can be used concomitantly.

Aufarbeitung

  1. customobtained
  2. customobtained

Quellen und Nachweise

ORD-Eintrag
ord-e6a644bd63d44275843be8afa42fd93a
Quelldatensatz
uspto-grants-1982_10
Patentnummer
US04352914

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