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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1,3-Diethyl 2-(1-oxopropyl)propanedioate | HCID 30720 | 89.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003663B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-b3787e9a769f4b7f882a91ee374fe0fc |
|---|
| Source note | uspto-grants-2011_08 |
|---|