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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495834Generated: October 30, 2026

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

https://huagongshe.com/reaction/495834

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 numberUS06939880B2
Source datasetuspto-grants-2005_09
ORD IDord-a3e5762f5c7a40a5b440ca618a1ef12c
Source noteuspto-grants-2005_09