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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919229Generated: November 3, 2026

Benzenesulfonyl chloride → N-(3-iodophenyl)benzenesulfonamide

https://huagongshe.com/reaction/1919229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant3-IodoanilineHCID 12271—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductN-(3-iodophenyl)benzenesulfonamideHCID 100999094%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3iodoaniline (5 g, 22.8 mmol), in CH2Cl2 (100 mL), were added at room temperature Et3N (6.97 mL) followed by benzenesulfonyl chloride (5.84 mL). The mixture was stirred 4 h then a white precipitate was formed. A saturated aqueous solution of NaHCO3 was added and the phases were separated. The aqueous layer was extracted several times with CH2Cl2 and the combined extracts were dried over (MgSO4) then evaporated. The crude mixture was dissolved in MeOH (100 mL) and NaOMe (6 g), was added and the mixture was heated 1 h at 60° C. The solution became clear with time and HCl (1N) was added. The solvent was evaporated under reduced pressure then the aqueous phase was extracted several times with CH2Cl2. The combined organic extracts were dried over (MgSO4) and evaporated. The crude material was purified by flash chromatography using (100% CH2Cl2) as solvent yielding the title compound 21 (7.68g, 94%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043343E1
Source datasetuspto-grants-2012_05
ORD IDord-888ca641c8ff4b99a0ccd688c7028d7d
Source noteuspto-grants-2012_05