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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582461Generated: November 1, 2026

Chloride → HCID 54079837, compound

https://huagongshe.com/reaction/582461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriethylamineHCID 8471—
ReactantHCID 54146006HCID 54146006—
SolventDichloromethaneHCID 6344—
ProductHCID 54079837HCID 54079837179.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.39 ml (5 mmol) of methenesulfonyl chloride dissolved in 5 ml of dichloromethane are added dropwise to a solution of 1.67 g (5 mmol) of N-tert-butyl-5-methylaminomethyl-2-methanesulfonylbenzenesulfonamide and 0.73 ml (5.3 mmol) of triethylamine in 20 ml of dichloromethane which had been cooled to 0° C. After 30 min at room temperature, the reaction solution is washed with water, dried and completely evaporated in vacuo. 1.85 g (89.7%) of N-tert-butyl-5-(N-methyl-N-methanesulfonylaminomethyl)-2-methanesulfonylbenzenesulfonamide are obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925596
Source datasetuspto-grants-1999_07
ORD IDord-acb46a44d0c84ea3b7996489567e793e
Source noteuspto-grants-1999_07