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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096574Generated: October 31, 2026

Hydrochloric Acid → HCID 86635070, compound

https://huagongshe.com/reaction/1096574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromophthalic anhydrideHCID 66590—
ProductHCID 86635070HCID 8663507022%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a 100 ml three-necked flask were added 6.42 g (28.3 mmol) of 4-bromophthalic anhydride (manufactured by Tokyo Chemical Industry Co. Ltd.), 25 ml of 10% fuming sulfuric acid, and 3.60 g (14.2=mol) of iodine. The mixture was heated to 110° C. and the reaction was carried out for 4 hours. After cooling at room temperature, the reaction mixture was poured into ice to quench the reaction. After the mixture was treated with a cold 20% aqueous sodium hydroxide solution, hydrochloric acid was added to adjust the pH of the solution to 6 to 7. Insoluble matter was removed by means of a filter paper and hydrochloric acid was added portionwise to adjust the pH to 1 or lower. After the resulting slurry was stirred overnight, the formed precipitate was filtrated and dried. The resulting solid was washed with toluene and the residue was treated with a cold 20% aqueous sodium hydroxide solution and dissolved therein. The pH of the solution was adjusted to 3.5 with acetic acid and the formed precipitate was removed by filtration. After the precipitate was treated with hydrochloric acid, the precipitate was further treated with toluene and acetic anhydride to obtain 1.10 g of 4-bromo-5-iodophthalic anhydride (yield 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138355B2
Source datasetuspto-grants-2012_03
ORD IDord-03bbd2b559e248aa95d9793ff5204a21
Source noteuspto-grants-2012_03