HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232655Generated: October 25, 2026
Sulfuric Acid → Diethyl 6-methyl-2,3,4,5-tetrafluorobenzoylmalonate
https://huagongshe.com/reaction/232655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2,3,4,5-Tetrafluoro-6-methylbenzoyl chloride | HCID 14651256 | — |
| Catalyst | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl 6-methyl-2,3,4,5-tetrafluorobenzoylmalonate | HCID 53783746 | — |
Reaction Steps
Separately, two drops of carbon tetrachloride are added to a solution of metallic magnesium (0.56 g) in absolute ethanol (0.9 ml). When the reaction starts, a mixture of diethyl malonate (3.6 ml), absolute ethanol (1.6 ml) and anhydrous toluene (6 ml) is added dropwise below 60° C. After stirring at 60° C. for 1 hour, the reaction mixture is cooled to 0° C. and thereto a solution of 6-methyl-2,3,4,5-tetrafluorobenzoyl chloride (5.00 g) prepared above in toluene (5 ml) is added dropwise. After stirring for 30 minutes, a mixture of conc. sulfuric acid (0.4 ml) and water (6 ml) is added and the mixture is extracted with diethyl ether, and the extract is dried over magnesium sulfate and concentrated to give diethyl 6-methyl-2,3,4,5-tetrafluorobenzoylmalonate (8 g) as an yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591744 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-65a61be3aa594242a939cfa817e15449 |
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| Source note | uspto-grants-1997_01 |
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