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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563125Generated: October 26, 2026

Potassium Iodide → Pap-1

https://huagongshe.com/reaction/563125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Bromobutoxy)benzeneHCID 70986—
ReactantBergaptolHCID 5280371—
SolventMethyl Ethyl KetoneHCID 6569—
ProductPap-1HCID 11302540—

Reaction Steps

700 mg (3.462 mmol) of 5-hydroxypsoralen (crystallized) and 600 mg (3.462 mmol) of 4-phenoxybutyl bromide was refluxed in 30 ml of 2-butanone in the presence of an excess (2 g) of anhydrous potassium carbonate and catalytic amounts of potassium iodide for 24 hours. The progress of the reaction was monitored by thin layer chromatography. After 24 hours the reaction mixture was concentrated under reduced pressure. The oily residue was cooled and diluted with water. The aqueous solution was then acidified with concentrated hydrochloric acid to pH 1. The slurry was stirred for 15-20 min and extracted with 3×100 ml of dichloromethane. The dichloromethane layer was extracted with 25 ml of 1% sodium hydroxide to separate the un-reacted 5-hydroxypsoralen. The dichloromethane layer was washed with 30 ml of 2% hydrochloric acid, dried over anhydrous sodium sulfate and concentrated. The solid residue was dissolved in a methanol-acetone mixture, treated with charcoal and re-crystallized from a methanol-acetone (80:20) mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067460B2
Source datasetuspto-grants-2011_11
ORD IDord-06720d0961244f34b97aa3f66f54abbd
Source noteuspto-grants-2011_11