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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650824Generated: October 26, 2026

Trifluoroacetic acid → N-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamide

https://huagongshe.com/reaction/650824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamic acid tert-butyl esterHCID 20677519—
SolventDichloromethaneHCID 6344—
ProductN-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamideHCID 1056133851.9%

Reaction Steps

At 0° C., trifluoroacetic acid (6 ml) was added to a solution of N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamic acid tert-butyl ester (870 mg, 2.6 mmol) in dichloromethane (6 ml). The reaction mixture was stirred for 50 min. Dichloromethane (24 ml) was added. A saturated aqueous solution of sodium hydrogen carbonate (34 ml) was added. Solid sodium hydrogen carbonate was added, until pH 7 was obtained. The phases were separated. The aqueous phase was extracted with dichloromethane (3×50 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash crhomatography on silica (60 g), using dichloromethane/methanol/25% aqueous ammonia (100:10:1) as eluent to give 308 mg of N-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274584B1
Source datasetuspto-grants-2001_08
ORD IDord-7728c890650447bdbdef7479c615b0c3
Source noteuspto-grants-2001_08