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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601998Generated: November 1, 2026

Trifluoroacetic acid → N-((2R)-2-methylamino-3-phenylpropyl)methansulfonamide

https://huagongshe.com/reaction/1601998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-((1R)-1-Benzyl-2-((methylsulfonyl)amino)ethyl)-N-methylcarbamic acid tert-butylesterHCID 54199950—
SolventDichloromethaneHCID 6344—
ProductN-((2R)-2-methylamino-3-phenylpropyl)methansulfonamideHCID 54473398101.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., trifluoroacetic acid (5 ml) was added to a solution of N-((1R)-1-benzyl-2-((methylsulfonyl)amino)ethyl)-N-methylcarbamic acid tert-butylester (913 mg, 2.67 mmol) in dichloromethane (5 ml). The reaction mixture was stirred for 15 min at 0° C. The solvent was removed in vacuo without warming. The residue was dissolved in dichloromethane (50 ml) and the solvent was removed in vacuo. The latter procedure was repeated two times. The crude product was purified by flash chromatography on silica (20 g), using dichloromethane/methanol/25% aqueous ammonia as eluent, to give 658 mg of N-((2R)-2-methylamino-3-phenylpropyl)methansulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977178
Source datasetuspto-grants-1999_11
ORD IDord-a80e089cad2b4efb837b9ddbaa41cdbd
Source noteuspto-grants-1999_11