HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359931Generated: November 1, 2026
Potassium Carbonate → Methyl 4-methyl-1-phenyl-1H-pyrrole-3-carboxylate
https://huagongshe.com/reaction/2359931
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | Methyl 4-methyl-1H-pyrrole-3-carboxylate | HCID 15274278 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-methyl-1-phenyl-1H-pyrrole-3-carboxylate | HCID 57687732 | 35% |
Reaction Steps
To a solution of methyl 4-methyl-1H-pyrrole-3-carboxylate (1.70 g) in N,N-dimethylformamide (1.5 mL) were added iodobenzene (1.50 mL), potassium carbonate (2.19 g), L-proline (273 mmg) and copper iodide (232 mg), and the reaction was carried out in a microwave reactor (Emrys Optimizer manufactured by Personal Chemistry, 70° C., 1 hr). The reaction mixture was filtered through celite, water was added to the filtrate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=9:1→2:1) to give the title compound as a colorless solid (yield 925 mg, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686010B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-37bafc78b2c840a5bac832e9ef79ddcf |
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| Source note | uspto-grants-2014_04 |
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