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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225977Generated: October 25, 2026

Potassium Iodide → 4-(3-Cyanopropoxy)-7H-furo[3,2-g][1]benzopyran-7-on

https://huagongshe.com/reaction/225977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-ChlorobutyronitrileHCID 12336—
ReactantBergaptolHCID 5280371—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-(3-Cyanopropoxy)-7H-furo[3,2-g][1]benzopyran-7-onHCID 11701730—

Reaction Steps

800 mg (3.956 mmol) of 5-hydroxypsoralen and 0.7 ml (655.5 mg, 6.33 mmol) of 4-chlorobutyronitrile were refluxed in 50 ml of 2-butanone in the presence of an excess (2.6 g) of anhydrous potassium carbonate and catalytic amounts of potassium iodide for 48 hours. The progress of the reaction was monitored by thin layer chromatography. After 48 hours the reaction mixture was concentrated under reduced pressure. The residual oily layer was cooled, diluted with water and acidified with concentrated hydrochloric acid to pH 1. The slurry was stirred for 15-20 min and then filtered. The solids were washed with water to neutral pH, dried bysuction and then further washed with petroleum ether. The dried solids were dissolved in refluxing methanol, treated with charcoal and recrystallized from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557138B2
Source datasetuspto-grants-2009_07
ORD IDord-1dbfc873fb324ad7975bc266acc8a3b3
Source noteuspto-grants-2009_07