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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423092Generated: October 25, 2026

Trifluoroacetic acid → 2-Amino-2-(4-chlorophenyl)ethanesulfonamide

https://huagongshe.com/reaction/423092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 1-(4-chlorophenyl)-2-sulfamoylethylcarbamateHCID 57750308—
Product2-Amino-2-(4-chlorophenyl)ethanesulfonamideHCID 5775036097.1%

Reaction Steps

Tert-butyl 1-(4-chlorophenyl)-2-sulfamoylethylcarbamate (Intermediate 79) (325 mg, 0.97 mmol) was treated with trifluoroacetic acid (8 mL). The resulting solution was stirred for 15 minutes at room temperature. The mixture was concentrated under reduced pressure and the residue was purified by ion exchange chromatography, using an SCX column. The column was washed with methanol and the desired product was eluted using ammonia in methanol (2M) and pure fractions were evaporated to dryness to afford 2-amino-2-(4-chlorophenyl)ethanesulfonamide (221 mg, 97%) as a near colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-c9bb3b2977934a038654faf21ae6b2ad
Source noteuspto-grants-2012_01