Reaktionsgleichung
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([CH2:12][C:13]([OH:15])=O)[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].S(Cl)([Cl:18])=O>>[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([CH2:12][C:13]([Cl:18])=[O:15])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5]Komponenten
3
Versuchsvorschrift
For conversion into the acid chloride, trans-4-pentylcyclohexylacetic acid (12.0 g, 0.0566 mol) was reacted for about 1 hour on an oil bath at 80° C. with thionyl chloride (50 ml). The solution obtained was evaporated under reduced pressure, treated with absolute toluene (50 ml) and once more evaporated under reduced pressure.
Aufarbeitung
- customThe solution obtained
- customwas evaporated under reduced pressure
- additiontreated with absolute toluene (50 ml)
- customonce more evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-f5c682759cb14903a7140f0f7b826a0a
- Quelldatensatz
- uspto-grants-1987_01
- Patentnummer
- US04637897
Verknüpfte Notizen
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