Methanol → HCID 86733722, Verbindung
Reaktionsgleichung
[CH3:1][C:2](/[CH:8]=[CH:9]\[CH2:10][CH:11]([CH3:18])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:17])[CH3:16])=[CH:3][C:4]([O:6]C)=[O:5].CO.[OH-].[K+]>O>[CH3:1][C:2](/[CH:8]=[CH:9]\[CH2:10][CH:11]([CH3:18])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:17])[CH3:16])=[CH:3][C:4]([OH:6])=[O:5]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 1 g. of trans/cis methyl 3,7,11-trimethyldodeca-2,4,10-trienoate, 60 ml. of methanol, 0.5 g. of potassium hydroxide and 6 ml. of water is heated at reflux for about 8 hours. The mixture is then diluted with water, neutralized and extracted with ether. The organic phase is washed with water, dried over sodium sulfate and evaporated to yield trans/cis 3,7,11-trimethyldodeca-2,4,10-trienoic acid.
Aufarbeitung
- additionA mixture of 1 g
- temperatureat reflux for about 8 hours
- extractionextracted with ether
- washThe organic phase is washed with water
- dry with materialdried over sodium sulfate
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-04c3820e25bb431284a37465ee557a9a
- Quelldatensatz
- uspto-grants-1976_07
- Patentnummer
- US03970704
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