Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423089Generated: October 25, 2026

Trifluoroacetic acid → N-[2-amino-2-(4-chlorophenyl)ethyl]methanesulfonamide

https://huagongshe.com/reaction/423089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 1-(4-chlorophenyl)-2-(methylsulfonamido)ethylcarbamateHCID 57750380—
ProductN-[2-amino-2-(4-chlorophenyl)ethyl]methanesulfonamideHCID 5775032487%

Reaction Steps

tert-butyl 1-(4-chlorophenyl)-2-(methylsulfonamido)ethylcarbamate (Intermediate 74) (151 mg, 0.43 mmol) was treated with trifluoroacetic acid (2 mL). The solution was stirred for 1 hour at room temperature. The mixture was concentrated under reduced pressure. The crude product was purified by ion exchange chromatography, using an SCX column. The residue was loaded onto the column in methanol and washed with methanol. The desired product was eluted from the column using 2M ammonia in methanol and pure fractions were evaporated to dryness to afford N-(2-amino-2-(4-chlorophenyl)ethyl)methanesulfonamide (93 mg, 86%) as a colourless crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-4a343d4eac324685964448e2906487cd
Source noteuspto-grants-2012_01