HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647849Generated: October 29, 2026
Chloroacetone → Diethyl (2-oxopropyl)propanedioate
https://huagongshe.com/reaction/1647849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl (2-oxopropyl)propanedioate | HCID 12000252 | 43.9% |
Reaction Steps
A solution of 25.0 g of diethyl malonate in 5 ml of dimethylformamide was added dropwise under ice-cooling over 20 minutes to a suspension of 6.55 g of sodium hydride in 90 ml of dimethylformamide. The reaction fluid was stirred for an hour under ice-cooling, to which a solution of 17.3 g of chloroacetone in 5 ml of dimethylformamide was added, and the mixture was stirred for an hour under ice-cooling and for 6 hours at room temperature. Ethyl acetate was added to the reaction fluid and the mixture was washed with water. The organic layer was dried over anhydrous magnesium sulfate. An oily matter obtained by concentrating the organic layer under a reduced pressure was distilled under vacuum to obtain 14.8 g of diethyl 2-oxopropylmalonate as a yellow oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434181 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-8c81e21be5614ca7807bb8172825cca0 |
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| Source note | uspto-grants-1995_07 |
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