Reaktionsgleichung
[C:1]([O:6][OH:7])([CH2:4][CH3:5])([CH3:3])[CH3:2].OC([C:12]1[CH:17]=[CH:16][C:15]([C:18]([OH:21])([CH3:20])[CH3:19])=[CH:14][CH:13]=1)(C)C.S(=O)(=O)(O)O>O>[C:1]([O:6][O:7][C:12]([C:13]1[CH:12]=[CH:17][CH:16]=[C:15]([C:18]([O:21][O:21][C:18]([CH2:15][CH3:14])([CH3:20])[CH3:19])([CH3:19])[CH3:20])[CH:14]=1)([CH3:17])[CH3:13])([CH2:4][CH3:5])([CH3:3])[CH3:2]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1,4-Bis(2-t-amylperoxy-2-propyl)benzene (para III) was prepared by reacting 28.1 grams (0.231 mole) of aqueous 85.7% t-amyl hydroperoxide diluted with 3.2 grams of water with 20.4 grams (0.105 mole) of 1,4-bis(2-hydroxy-2-propyl)benzene in the presence of 44.1 grams (0.316 mole) of 70% sulfuric acid according to the procedure of Example VII. The stripped product was a yellow liquid which remained liquid at 15° C. The product weighed 32.0 grams.
Aufarbeitung
- customat 15° C
Quellen und Nachweise
- ORD-Eintrag
- ord-ccabd420d1484ab6a9d0f8a6e1052f08
- Quelldatensatz
- uspto-grants-1998_02
- Patentnummer
- US05719096
Verknüpfte Notizen
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