HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526457Generated: October 27, 2026
Dimethyl malonate → HCID 117600964, compound
https://huagongshe.com/reaction/526457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 4-Bromo-2-fluoro-5-methylbenzonitrile | HCID 34175419 | — |
| Catalyst | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117600964 | HCID 117600964 | 43.1% |
Reaction Steps
Combined 4-bromo-2-fluoro-5-methylbenzonitrile (4 g, 18.69 mmol) and dimethyl malonate (29.9 mL, 262 mmol) and purged with nitrogen. Potassium carbonate (3.87 g, 28.0 mmol), potassium hydrogencarbonate (2.81 g, 28.0 mmol), tri-tert-butylphosphonium tetrafluoroborate (0.119 g, 0.411 mmol), and bis(dibenzylidineacetone)palladium(0) (0.118 g, 0.206 mmol) were added. The reaction mixture was then heated in an oil bath at 170° C. After 3 hours, the reaction mixture was cooled, diluted with ethyl acetate, and filtered through Celite®. The filtrate was concentrated and the residue dissolved in EtOAc. The organic solution was washed with 1N aqueous sodium hydroxide (2×), twice with 10% aqueous sodium chloride, and then brine. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue which was purified by flash chromatography to give the title compound (1.67 g, 43%) as a clear colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.30 (s, 3H) 3.67 (s, 2H) 3.72 (s, 3H) 7.10 (d, J=9.60 Hz, 1H) 7.42 (d, J=6.32 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345713B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-344e64a6b9c041d9a9674f48467c6edf |
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| Source note | uspto-grants-2016_05 |
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