HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054721Generated: October 27, 2026
Picolinic acid → Diethyl 2-(4-bromo-2-methoxyphenyl)malonate
https://huagongshe.com/reaction/1054721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Picolinic acid | HCID 1018 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Reactant | 4-Bromo-1-iodo-2-methoxybenzene | HCID 46835731 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | Diethyl 2-(4-bromo-2-methoxyphenyl)malonate | HCID 86698720 | — |
Reaction Steps
A mixture of 4-bromo-1-iodo-2-methoxybenzene (1100 mg, 3.5 mmol), diethylmalonate (1240 mg, 7.70 mmol), cesium carbonate (1830 mg, 5.60 mmol), 2-picolinic acid (62 mg, 0.39 mmol), copper (I) iodide (34 mg, 0.18 mmol), and dioxane (7 ml) was stirred at 55° C. for 2 days. A very heavy slurry formed, LCMS indicates that the starting iodoarene is about 70% consumed. The mixture was cooled to room temperature and diluted with 30 mL of water and extracted with ethyl acetate. The extract was washed with water, brine, dried over magnesium sulfate, and concentrated to obtain the title compound which was about 60% pure by LCMS and was used for the next step without purification. GCMS (ES+) 344 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394285B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-38b3b7a36d8e469bbab438dd1175e3be |
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| Source note | uspto-grants-2016_07 |
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