HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266548Generated: October 27, 2026
Hydrochloric Acid → HCID 54118611, compound
https://huagongshe.com/reaction/266548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Nitro-4-(trifluoromethyl)benzoyl chloride | HCID 14323524 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 54118611 | HCID 54118611 | 96.2% |
Reaction Steps
A mixture of magnesium turnings (4.94 g) and carbon tetrachloride (2 ml) in ethanol (35 ml) was warmed to 50° C. until the reaction started. Diethyl ether (150 ml) was then added cautiously, with stirring. A solution of diethyl malonate (32.5 g) in diethyl ether (50 ml) was then added dropwise, then stirred and heated at reflux for 2 hours. After cooling the mixture, diethyl ether (150 ml) was added. A solution of 2-nitro-4-trifluoromethylbenzoyl chloride (50.7 g) in diethyl ether (100 ml) was added dropwise. The mixture was heated at reflux for 2 hours. After cooling, hydrochloric acid (2M,200 ml) was added and the layers were separated. The organic layer was washed with water, dried (anhydrous sodium sulphate), and filtered. The filtrate was evaporated to dryness, to give diethyl 2-nitro-4-trifluoromethylbenzoylmalonate (72.6 g), in the form of an off-white solid, m.p. 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650533 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-b653957c0a7443a0b7b9692037e38a2d |
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| Source note | uspto-grants-1997_07 |
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