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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962315Generated: November 1, 2026

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

https://huagongshe.com/reaction/1962315

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 numberUS08415351B2
Source datasetuspto-grants-2013_04
ORD IDord-3d9f19e0ab884101882221c14d22c05b
Source noteuspto-grants-2013_04