Sulfuric Acid → Cyclohexaneacetic acid, 3,3,5-trimethyl-
Reaktionsgleichung
[CH3:1][C:2]1([CH3:15])[CH2:7][CH:6]([CH3:8])[CH2:5][CH:4]([CH2:9][C:10]([O:12]CC)=[O:11])[CH2:3]1.[OH-].[Na+].S(=O)(=O)(O)O>O>[CH3:15][C:2]1([CH3:1])[CH2:7][CH:6]([CH3:8])[CH2:5][CH:4]([CH2:9][C:10]([OH:12])=[O:11])[CH2:3]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
875 g of ethyl 3,3,5-trimethyl-cyclohexylacetate are treated in 2.2 l of water with 670 g of 30% sodium hydroxide and the mixture is held at reflux temperature for 21/2 hours while stirring. After cooling, the mixture is neutralized, acidified with 420 g of 63% sulphuric acid and extracted with cyclohexane. The cyclohexane extract is washed neutral, evaporated and the 770 g of crude product are distilled. There are obtained 630 g of 3,3,5-trimethyl-cyclohexylacetic acid. (Yield: 82%).
Aufarbeitung
- temperatureat reflux temperature for 21/2 hours
- temperatureAfter cooling
- extractionextracted with cyclohexane
- extractionThe cyclohexane extract
- washis washed neutral
- customevaporated
- distillationthe 770 g of crude product are distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-7d55fbf5e5534c99b9480ca9485b6e28
- Quelldatensatz
- uspto-grants-1984_07
- Patentnummer
- US04457862
Notizen zur Reaktion
Wird geladen…