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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675650Generated: October 30, 2026

Hydrochloric Acid → 1,3-Diethyl 2-(1-oxopropyl)propanedioate

https://huagongshe.com/reaction/1675650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantPropionyl chlorideHCID 62324—
ReactantMagnesium ChlorideHCID 5360315—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product1,3-Diethyl 2-(1-oxopropyl)propanedioateHCID 3072089.1%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

To a mixture of diethyl malonate (704 g, e.g. available from Spectrochem) and acetonitrile (3.8 L) was added anhydrous magnesium chloride immediately (419 g, e.g. available from Lancaster). Triethylamine (1222 ml) was added dropwise, maintaining the temperature at 5-10° C., followed by the dropwise addition of propionyl chloride (406 g), maintaining the temperature at or below 30° C. The reaction mixture was kept at 10-15° C. for 1 hour, and then the mixture was kept overnight at room temperature. The next day, aqueous hydrochloric acid (1 M) was added to the reaction mixture until the pH of the mixture was about 2.0 (approx. 4.8 L was required). The mixture was extracted with diethyl ether (3×800 ml). The combined ethereal extracts were washed with aqueous hydrochloric acid (1M, 2×1000 ml), followed by water (2×1000 mL) and finally with brine (2×1000 mL). Evaporation of the solvent from the ethereal extracts under reduced pressure afforded diethyl propanoylpropanedioate (845 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003663B2
Source datasetuspto-grants-2011_08
ORD IDord-b3787e9a769f4b7f882a91ee374fe0fc
Source noteuspto-grants-2011_08