HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810440Generated: October 31, 2026
Dichloromethane → 2-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester
https://huagongshe.com/reaction/1810440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dibromo-5-chlorobenzene | HCID 84676 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester | HCID 57458806 | — |
Reaction Steps
1,3-Dibromo-5-chlorobenzene (25 g, 93 mmol), dimethyl malonate (23.4 mL, 204 mmol), and copper(I) bromide (29.2 g, 204 mmol) were combined in 1,4-dioxane (300 mL) and cooled to 0° C. Sodium hydride (60% in mineral oil; 8.2 g, 204 mmol) was added slowly, and the reaction was stirred at room temperature for 20 minutes, and then stirred at 105° C. for 4 hours. After cooling to room temperature, the mixture was worked-up with CH2Cl2 and aqueous Na4OH. The organic layer was concentrated, and the residue was purified by silica gel chromatography (0-20% EtOAc in hexanes) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362044B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-0b3b28226926445b8a8427309a70b440 |
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| Source note | uspto-grants-2013_01 |
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