HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487171Generated: November 1, 2026
Diethyl Malonate → Triethyl propane-1,1,2-tricarboxylate
https://huagongshe.com/reaction/1487171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Triethyl propane-1,1,2-tricarboxylate | HCID 242462 | 84% |
Reaction Steps
To a solution of anhydrous ethanol (500 mL) was added sodium (9 g, 0.39 mol) in pieces. After all the sodium dissolved, diethyl malonate (50 g, 0.31 mol) was added dropwise at 0° C., and the mixture was stirred at 0° C. for another 30 minutes, followed by the addition of (±)-ethyl 2-bromopropanoate (56.5 g, 0.31 mol) dropwise. The mixture was warmed to room temperature for 1 hour and then heated at reflux for 12 hours. After cooling to room temperature, most of solvents were removed, and the residue was diluted with ethyl acetate. The organic phase was washed by brine, dried over anhydrous sodium sulfate and evaporated to afford the product (±)-triethyl propane-1,1,2-tricarboxylate (67.8 g, yield 83.4%), which was used for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428508B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4b891eb2f3f34917afbcce568246b571 |
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| Source note | uspto-grants-2016_08 |
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