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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905045Generated: October 30, 2026

Benzene → HCID 13151225, compound

https://huagongshe.com/reaction/905045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Propenoic acid, 2,3,3-triiodo-HCID 5325140—
ProductHCID 13151225HCID 13151225—

Reaction Steps

A solution of 0.3 ml of thionyl chloride in 2 ml of benzene was added dropwise to a mixture of 0.3 g of triiodoacrylic acid, 0.3 ml of pyridine and 3 ml of benzene. The mixture was then stirred at room temperature for 45 minutes, after which the solvent was distilled off under reduced pressure. 5 ml of benzene and 0.3 ml of pyridine were added to the resulting residue, and then 0.3 g of phenol was added, with ice-cooling, after which the mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was poured into an ice-cooled dilute solution of hydrochloric acid and then extracted with diethyl ether. The extract was washed, in turn, with a saturated aqueous solution of sodium bicarbonate, water and then a saturated aqueous solution of sodium chloride. The resulting solution was dried over anhydrous sodium sulphate and then the solvent was distilled off under reduced pressure. The resulting residue was purified by column chromatography through silica gel eluted with a 100:12 by volume mixture of hexane and ethyl acetate, to give 0.18 g of the title compound, melting at 83°-84.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04421766
Source datasetuspto-grants-1983_12
ORD IDord-7e05995589f9473ead3777f209c60b46
Source noteuspto-grants-1983_12