Reaktionsgleichung
[F:1][C:2]([F:31])([F:30])[S:3]([CH:6]([S:23]([C:26]([F:29])([F:28])[F:27])(=[O:25])=[O:24])[CH2:7][CH:8](S(C(F)(F)F)(=O)=O)S(C(F)(F)F)(=O)=O)(=[O:5])=[O:4].[C:32]1([C:38]2[CH:43]=[CH:42]C=[C:40]([C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)[C:39]=2[OH:50])[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>C(#N)C>[F:27][C:26]([F:28])([F:29])[S:23]([CH:6]([S:3]([C:2]([F:31])([F:30])[F:1])(=[O:5])=[O:4])[CH2:7][C:8]1[C:40]([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)=[C:39]([OH:50])[C:38]([C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)=[CH:43][CH:42]=1)(=[O:24])=[O:25]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1,1,3,3-Tetrakis(trifluoromethylsulfonyl)propane [4] (157.3 mg, 0.28 mmol) was added to an acetonitrile (0.25 ml) solution of 2,6-diphenylphenol (61.9 mg, 0.25 mmol) at room temperature. After 9 hours of stirring, it was purified by Kugelrohr distillation (120° C./3 mmHg) thereby obtaining 4-(2,2-bis(trifluoromethylsulfonyl)ethyl-2,6-diphenylphenol [1n] with a yield of 97% (130.7 mg, 0.24 mmol).
Aufarbeitung
- distillationit was purified by Kugelrohr distillation (120° C./3 mmHg)
Quellen und Nachweise
- ORD-Eintrag
- ord-848fe28437874a8395a0f0132f1f7fd1
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09314782B2
Verknüpfte Notizen
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