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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797835Generated: November 3, 2026

Water → 4-iodo-N-(2-hydroxyphenyl)benzamide

https://huagongshe.com/reaction/1797835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-AminophenolHCID 5801—
ReactantTriethylamineHCID 8471—
Reactant4-Iodobenzoyl chlorideHCID 74373—
SolventTetrahydrofuranHCID 8028—
Product4-iodo-N-(2-hydroxyphenyl)benzamideHCID 1635099497%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 300 mL three-neck flask were put 10 g (92 mmol) of 2-aminophenol and 7.0 mL of triethylamine and was added 100 mL of tetrahydrofuran (THF). The solution was stirred at 0° C. for 20 minutes. After the stirring, a solution in which 0.10 mol of 4-iodobenzoyl chloride was dissolved in 100 mL of tetrahydrofuran (THF) was dropped. The solution was stirred at 0° C. for 5 hours under a nitrogen stream. After the stirring, the solution was added to about 300 mL of water and an aqueous layer of the obtained mixture was extracted with ethyl acetate. After the extraction, the extracted solution was combined with the organic layer and washed with 1 M hydrochloric acid, a saturated aqueous solution of sodium hydrogen carbonate and brine in this order. After the washing, magnesium sulfate was added into the organic layer to dry the organic layer. After the drying, the mixture was subjected to suction filtration through Celite (manufactured by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855) to give a filtrate. The solid, which was obtained by condensation of the obtained filtrate, was recrystallized with a mixed solvent of ethyl acetate and hexane to give 30 g of a powdery white solid in a yield of 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343639B2
Source datasetuspto-grants-2013_01
ORD IDord-fe3b3219f87b41448e1c9f1730cfeed6
Source noteuspto-grants-2013_01