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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488443Generated: November 3, 2026

Potassium Iodide → HCID 16178995, compound

https://huagongshe.com/reaction/1488443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantN-3-BromopropylphthalimideHCID 21611—
Reactant5,10,15,20-Tetrakis(3-hydroxyphenyl)porphyrinHCID 135462976—
SolventDimethylformamideHCID 6228—
ProductHCID 16178995HCID 16178995—

Reaction Conditions

Temperature21 °C

Reaction Steps

7.56 g (11.14 mmol) of 5,10,15,20-tetrakis-(3-hydroxyphenyl)-porphyrin [CARN 22112-79-4] is dissolved in 300 ml of anhydrous N,N-dimethylformamide and mixed with 30.79 g (222.8 mmol) of potassium carbonate and 7.40 g (44.55 mmol) of potassium iodide. 59.72 g (222.8 mmol) of N-(3-bromopropyl)-phthalimide is added to the suspension that is stirred under argon at 21° C. After 24 hours of stirring with exclusion of light, the suspension is filtered, the filtrate is largely concentrated by evaporation in a vacuum, mixed with dichloromethane and shaken out twice with water. The organic phase is dried on anhydrous magnesium sulfate, filtered and concentrated by evaporation, the residue is chromatographed on silica gel 60 (Merck) with dichloromethane/methanol. The product fractions are concentrated by evaporation, taken up in a little dichloromethane and the title compound is precipitated by the addition of diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674467
Source datasetuspto-grants-1997_10
ORD IDord-8c5d591e9abd4d1187d7067ac7c704d3
Source noteuspto-grants-1997_10