HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232634Generated: October 26, 2026
Sulfuric Acid → Diethyl 2-(3-bromo-2-chloro-4,5-difluorobenzoyl)malonate
https://huagongshe.com/reaction/2232634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Magnesium ethanolate | HCID 164963 | — |
| Reactant | 3-Bromo-2-chloro-4,5-difluorobenzoyl chloride | HCID 14071797 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl 2-(3-bromo-2-chloro-4,5-difluorobenzoyl)malonate | HCID 14071798 | 104.8% |
Reaction Steps
To the magnesium ethoxide (3.93 g) suspension was added a solution of diethyl malonate (4.65 g) in anhydrous toluene (30 ml) dropwise during 25 minutes at 20° to 25° C. The mixture was stirred at 50° to 60° C. for 3 hours, and then cooled in an acetone-dry ice bath. A solution of 3-bromo-2-chloro-4,5-difluorobenzoyl chloride (7.65 g) in anhydrous toluene (15 ml) was added dropwise to the resulting solution at -16° to 0° C. during 25 minutes. The mixture was stirred for 2.5 hours below 0° C., then further stirred at room temperature for 40 minutes, and then mixed with ice water (15 ml) containing concentrated sulfuric acid (1 ml). The resulting organic layer was collected and the water layer was extracted with toluene. The combined organic layer was washed with water, dried over anhydrous sodium sulfate and then concentrated to give the title compound (11.44 g) as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04788320 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-037f4d372bad4e72a30ad8f78fd723e9 |
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| Source note | uspto-grants-1988_11 |
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