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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482988Generated: October 31, 2026

Iodine → HCID 20244553, compound

https://huagongshe.com/reaction/482988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantDibenzoylmethaneHCID 8433—
Reactant2-Cyclopropen-1-oneHCID 137779—
Reactant2-Cyclopropen-1-one, 2,3-bis(4-methoxyphenyl)-HCID 12290270—
ProductHCID 20244553HCID 2024455395%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 10 percent solution of 2,3-di(4-methoxyphenyl)cyclopropenone in pyridine was refluxed under nitrogen for 15 minutes. The resulting solution was cooled slightly, and an equivalent amount of dibenzoylmethane based on the cyclopropenone was added to the green solution. The reaction mixture was refluxed for 60 minutes. The resulting reaction mixture was again cooled, and four equivalents of iodine dissolved in a small amount of pyridine was added to the reaction mixture. The mixture was further heated at 90° C. on a steam bath for 15 minutes. The bright blue solution was quenched by pouring it into cold excess dilute hydrochloric acid. The desired dye precipitated and was removed from the solution by filtering. A 95 percent yield of the desired dye was obtained based on the starting cyclopropenone. The dye was chromatographed on silica gel to provide a purified product. The maximum absorption of the dye was at 605 nm in chloroform solution. The structure of the dye was confirmed by mass spectroscopy, nuclear magnetic resonance and infrared analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04577024
Source datasetuspto-grants-1986_03
ORD IDord-572ae08e1bb94f0ca09b1ff03877e184
Source noteuspto-grants-1986_03