Reaktionsgleichung
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([C:12]([OH:14])=[O:13])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].[F:15][C:16]([F:25])([F:24])[C@H:17]1[CH2:22][CH2:21][C@H:20](O)[CH2:19][CH2:18]1>>[CH2:1]([C@H:6]1[CH2:7][CH2:8][C@H:9]([C:12]([O:14][C@H:20]2[CH2:21][CH2:22][C@H:17]([C:16]([F:25])([F:24])[F:15])[CH2:18][CH2:19]2)=[O:13])[CH2:10][CH2:11]1)[CH2:2][CH2:3][CH2:4][CH3:5]Komponenten
3
Versuchsvorschrift
0.005 mol of trans-4-pentylcyclohexanecarboxylic acid are esterified analogously to Example 4 using 0.005 mol of trans-4-trifluoromethylcyclohexanol (prepared as in Example 2). The product is obtained as a colourless solid.
Aufarbeitung
- customThe product is obtained as a colourless solid
Quellen und Nachweise
- ORD-Eintrag
- ord-39b6d9d6b8bc4bb3b5be7cc9150437fa
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05209868
Verknüpfte Notizen
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