Reaktionsgleichung
[C:1]1([CH:7](O)[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:11]>O>[Cl:11][CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH2:8][CH3:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
13.6 g (0.1 mole) of 1-phenylpropan-1-ol are taken up in petroleum ether and are reacted at -20° C. with hydrochloric acid until the precipitation of water is terminated. Subsequently, the organic phase is washed neutral with water, dried (sodium sulfate) and the petroleum ether removed in a vacuum. The bright yellow, thermolabile oil is used without further purification. The oil has an Rf of 0.8 (CH2Cl2) and is attained in a yield of 13.1 g (85%).
Aufarbeitung
- customis terminated
- washSubsequently, the organic phase is washed neutral with water
- dry with materialdried (sodium sulfate)
- customthe petroleum ether removed in a vacuum
- customThe bright yellow, thermolabile oil is used without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-dcd316a38b4f4ea7a34c064d42946357
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04764533
Verknüpfte Notizen
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