Hydrochloric Acid → Ethyl 2-ethoxycarbonyl-3,3-dimethylhexanoate

Temperature

-50 °C

To a solution of n-propylmagnesium bromide in THF (1.62N, 149 ml, 242 mmol), anhydrous THF (200 ml) was added and the mixture was cooled to -50° C. After adding hydrated copper acetate (2.42 g, 12.1 mmol), a solution of diethyl isopropylidenemalonate (22 g, 110 mmol) in anhydrous THF (100 ml) was slowly added to the solution at -50° C., and the mixture was stirred at -50° C. for 2 hours. Aqueous hydrogen chloride (1N, 260 ml) was added at room temperature and the mixture was extracted with ethyl acetate (500 ml, 100 ml×3). Aqueous saturated solution of sodium hydrogencarbonate (100 ml) was added to the combined organic layers and filtered. The aqueous layer was separated from the organic layer of the filtrate. The organic layer was washed with brine (300 ml), dried over magnesium sulfate, and concentrated. The residue was distilled under reduced pressure to give ethyl 2-ethoxycarbonyl-3,3-dimethylhexanoate (24.92 g, 102 mmol, 92.7%, b.p.: 85°-87° C./1 mmHg). The structure was identified by the following data.

1. extractionthe mixture was extracted with ethyl acetate (500 ml, 100 ml×3)
2. additionAqueous saturated solution of sodium hydrogencarbonate (100 ml) was added to the combined organic layers
3. filtrationfiltered
4. customThe aqueous layer was separated from the organic layer of the filtrate
5. washThe organic layer was washed with brine (300 ml)
6. dry with materialdried over magnesium sulfate
7. concentrationconcentrated
8. distillationThe residue was distilled under reduced pressure

ORD record

ord-34323b772c3247c283c5d2938b07d382

Source dataset

uspto-grants-1988_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04775692