HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297631Generated: October 30, 2026
Dimethylformamide → 4-Ethoxy-6-formyl-quinoline-3-carbonitrile
https://huagongshe.com/reaction/1297631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | CID 76231 | HCID 76231 | — |
| Reactant | HCID 58585794 | HCID 58585794 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Diphenylpropyl phosphine | HCID 53436545 | — |
| Product | 4-Ethoxy-6-formyl-quinoline-3-carbonitrile | HCID 58585818 | 51% |
Reaction Steps
A mixture of 4-ethoxy-6-iodo-quinoline-3-carbonitrile (example 14d, 6.4 g, 20 mmol), trethylamine (6.9 mL, 50 mmol), diphenylpropylphosphine (dpp, 0.23 uL, 1 mmol) and palladium(II) acetate (0.22 g, 1 mmol) in dry N,N-dimethylformamide (120 mL) in pressure tube was stirred under carbon monoxide at 75 psi at room temperature for 10 min. After addition of trihexylsilane (14 mL, 40 mmol), the mixture was then stirred under carbon monoxide at 75 psi at 80° C. for 3 h. The reaction was allowed to cool to 25° C. and then extracted with ethyl acetate (2×200 mL). The combined organic layers were successively washed with a saturated aqueous sodium bicarbonate solution (3×50 mL) and water (3×50 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 5%-40% ethyl acetate in hexanes in 30 min) afforded 4-ethoxy-6-formyl-quinoline-3-carbonitrile (2.3 g, 51%) as a white solid. LC-MS m/e 227 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250515B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-bb594acf1ddd4214a441d87241a63da2 |
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| Source note | uspto-grants-2007_07 |
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