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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463330Generated: October 27, 2026

Triethylamine → N-(4-nitrobenzyl)methanesulfonamide

https://huagongshe.com/reaction/1463330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Nitrobenzylamine hydrochlorideHCID 11252467—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-(4-nitrobenzyl)methanesulfonamideHCID 1282252085%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 25.0 g (133 mmol, 1.0 equiv.) of 4-nitro benzylamine hydrochloride in 500 mL of methylene chloride at 0° C. was added 46.4 mL (331 mmol, 2.5 equiv.) of triethylamine followed by 11.3 mL (146 mmol, 1.1 equiv.) of methanesulfonyl chloride dropwise. The reaction was stirred for thirty minutes at 0° C. then diluted with 500 mL of chloroform. The organic layer was washed with 150 mL portions of 1N HCl and saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated to give 25.8 g (85%) of N-[(4-nitrophenyl)methyl]methanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300506
Source datasetuspto-grants-1994_04
ORD IDord-edd256646853408ca89f6d014932bad0
Source noteuspto-grants-1994_04