HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297620Generated: October 30, 2026
Dimethylformamide → 6-Formyl-4-ethoxy-quinoline-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1297620
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | CID 76231 | HCID 76231 | — |
| Reactant | Diphenylpropyl phosphine | HCID 53436545 | — |
| Reactant | 6-Iodo-4-ethoxy-quinoline-3-carboxylic acid ethyl ester | HCID 68828458 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 6-Formyl-4-ethoxy-quinoline-3-carboxylic acid ethyl ester | HCID 58585809 | 59% |
Reaction Steps
A mixture of 6-iodo-4-ethoxy-quinoline-3-carboxylic acid ethyl ester (example 9a) (0.58 g, 1.56 mmol), triethylamine (0.54 mL, 3.91 mmol), diphenylpropylphosphine (dpp, 36 uL, 0.16 mmol) and palladium(II) acetate (35 mg, 0.16 mmol) in dry N,N-dimethylformamide (16 mL) in pressure tube was stirred under carbon monoxide at 75 psi at room temperature for 10 min. After addition of trihexylsilane (1.11 mL, 3.13 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 methylene chloride (2×100 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, 0%-40% ethyl acetate in hexanes in 30 min) afforded 6-formyl-4-ethoxy-quinoline-3-carboxylic acid ethyl ester (0.25 g, 59%) as a white solid.
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-10f4241323a6436b9ab4114de267a3b2 |
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| Source note | uspto-grants-2007_07 |
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