Hydrochloric Acid → Ethyl 2,2-dimethylbutanoate
Reaktionsgleichung
Cl.[CH3:2][C:3]([CH3:9])([CH2:7][CH3:8])[C:4]([OH:6])=[O:5].O.[CH2:11](O)[CH3:12]>>[CH2:11]([O:5][C:4](=[O:6])[C:3]([CH3:9])([CH3:2])[CH2:7][CH3:8])[CH3:12]Komponenten
5
Versuchsvorschrift
Add 0.2 mL of concentrated hydrochloric acid to 2,2-dimethyl-butanoic acid (5.0 g, 43.0 mmol) in ethanol (43 mL) and heat to reflux for 5 hours. Cool to room temperature. Pour the reaction into water and extract with diethyl ether. Wash the combined organics with saturated aqueous sodium bicarbonate and water, dry over magnesium sulfate, filter, and concentrate under reduced pressure to afford the title compound which was used without further purification (4.0 g, 64.4%): 1H NMR (CDCl3) δ 0.82 (t, 3H, 1.14 (s, 3H), 1.23 (t, 3H), 1.55 (q, 2H), 4.1 (q, 2H).
Aufarbeitung
- temperatureheat
- temperatureto reflux for 5 hours
- additionPour
- extractionextract with diethyl ether
- washWash the combined organics with saturated aqueous sodium bicarbonate and water
- dry with materialdry over magnesium sulfate
- filtrationfilter
- concentrationconcentrate under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-59e87af6c13d4a4197ab5e5aa2efb6b9
- Quelldatensatz
- uspto-grants-2013_11
- Patentnummer
- US08592590B2
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