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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867765Generated: October 30, 2026

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

https://huagongshe.com/reaction/867765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantDiethyl isopropylidenemalonateHCID 81255—
ReactantHCID 178455851HCID 178455851—
ProductEthyl 2-ethoxycarbonyl-3,3-dimethylhexanoateHCID 1430217592.7%

Reaction Conditions

Temperature-50 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775692
Source datasetuspto-grants-1988_10
ORD IDord-34323b772c3247c283c5d2938b07d382
Source noteuspto-grants-1988_10