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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360022Generated: October 31, 2026

Pyridine → N-(4-iodo-3-methylphenyl)methanesulfonamide

https://huagongshe.com/reaction/2360022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Iodo-3-methylanilineHCID 2734275—
SolventDichloromethaneHCID 6344—
ProductN-(4-iodo-3-methylphenyl)methanesulfonamideHCID 5879897994.3%

Reaction Steps

A solution of 4-iodo-3-methylaniline (4.37 g, 18.75 mmol) in CH2Cl2 (25 ml) was treated with pyridine (6.07 ml, 75 mmol) followed by drop wise addition of methanesulfonyl chloride (1.607 ml, 20.63 mmol) to give a reddish/orange mixture. The mixture was stirred for 2 h, concentrated and diluted with EtOAc. The EtOAc layer was washed with 1M HCl, water, saturated NaCl, dried (Na2SO4) and filtered. The EtOAc filtrate was treated with activated charcoal for 30 min at 50° C. and filtered through a 10 g silica plug and concentrated to give the title compound as a light yellow solid (5.5 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685991B2
Source datasetuspto-grants-2014_04
ORD IDord-09445becf34c49499f76b42a32117034
Source noteuspto-grants-2014_04