HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339141Generated: October 25, 2026
Ethyl chloroacetate → Triethyl ethane-1,1,2-tricarboxylate
https://huagongshe.com/reaction/339141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triethyl ethane-1,1,2-tricarboxylate | HCID 81961 | — |
Reaction Steps
Sodium metal (23 gram, 1 mole) was dissolved in dry ethanol (500 ml) with stirring. To this 160 gram (1 mole) of diethyl malonate (compound [2]) was added in 30 minutes. The reaction mixture was cooled to 15° C. and ethyl chloroacetate (compound [1], 117 gm, 0.095 mole) was then added drop wise in 30 minutes. On completion of addition the reaction mass was refluxed for 6 hours and then poured in 2 liters of water. The organic materials were extracted with dichloromethane (three times with 500 ml). Next, the organic extracts were dried over sodium sulfate, filtered and evaporated to give an oily substance which was then vacuum distilled to give 220 gm (89% of the theoretical maximum yield) of triethyl ethane-1,1,2-tricarboxylate, compound [3].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889898B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-86c9e29abcc54df4b18a6630f6d32b65 |
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| Source note | uspto-grants-2014_11 |
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