HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428732Generated: October 31, 2026
Sodium Carbonate → 2-m-Tolyl-6-(trifluoromethyl)nicotinonitrile
https://huagongshe.com/reaction/1428732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Tolylboronic acid | HCID 2733950 | — |
| Reactant | 2-Chloro-6-(trifluoromethyl)nicotinonitrile | HCID 2778413 | — |
| Reactant | Cyclohexane ethylacetate | HCID 21867204 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-m-Tolyl-6-(trifluoromethyl)nicotinonitrile | HCID 86680215 | 49% |
Reaction Steps
2-Chloro-6-(trifluoromethyl)nicotinonitrile (3 g, 14.56 mmol) was dissolved in toluene (70 mL) and ethanol (14 mL). m-tolylboronic acid (2.969 g, 21.814 mmol), aqueous sodium carbonate solution (2 M, 14 mL) and Pd(PPh3)4 (1.684 g, 1.456 mmol) were added. The mixture was flushed with nitrogen and stirred under microwave conditions (7 bar) at 100° C. for 2 h. The concentrated reaction mixture was cooled, diluted with ethyl acetate (200 mL), passed through celite (cyclohexane/ethyl acetate 9:1, 2×1 L) and concentrated in vacuo to afford 2-m-tolyl-6-(trifluoromethyl)nicotinonitrile (1.87 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937092B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-6f30511677c749ccbacfa832fd2b2618 |
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| Source note | uspto-grants-2015_01 |
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