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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843320Generated: October 30, 2026

Potassium Iodide → Quinoline-6-carboxylic acid oxiranylmethyl ester

https://huagongshe.com/reaction/843320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Quinolinecarboxylic acidHCID 82571—
SolventDimethylformamideHCID 6228—
ProductQuinoline-6-carboxylic acid oxiranylmethyl esterHCID 1202026421.1%

Reaction Steps

Quinoline-6-carboxylic acid (1 g; 5.78 mmol) is dissolved in DMF (10 mL) at ambient temperature. Epichlorohydrin (0.4517 mL; 5.59 mmol) is added followed by mortar ground potassium carbonate (0.80 g; 5.79 mmol). The mixture is stirred at ambient temperature for 48 hours. Potassium iodide (96 mg; 0.58 mmol) is added and stirring is continued at ambient temperature for 24 hours. The mixture is heated to 60° C. and maintained for 72 hours. After cooling, the mixture is poured onto water (700 mL) and extracted with ethyl acetate (3×100 mL). The combined organic extracts are washed successively with water (100 mL), and brine (50 mL), then dried over MgSO4, filtered, and concentrated in vacuo at 30C. The residue is purified via silica gel chromatography with gradient elution (20%→67% ethyl acetate in hexanes) affording the desired product (270 mg) as a white solid. ESMS: MH+ 230.0 (base).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376514B1
Source datasetuspto-grants-2002_04
ORD IDord-048b0799dc664b1aa3fe5190d3516354
Source noteuspto-grants-2002_04