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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantCID 76231HCID 76231—
ReactantDiphenylpropyl phosphineHCID 53436545—
Reactant6-Iodo-4-ethoxy-quinoline-3-carboxylic acid ethyl esterHCID 68828458—
Catalystpalladium(II) acetateHCID 167845—
Product6-Formyl-4-ethoxy-quinoline-3-carboxylic acid ethyl esterHCID 5858580959%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250515B2
Source datasetuspto-grants-2007_07
ORD IDord-10f4241323a6436b9ab4114de267a3b2
Source noteuspto-grants-2007_07