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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423123Generated: October 30, 2026

Trifluoroacetic acid → N-[3-amino-3-(4-chlorophenyl)propyl]methanesulfonamide

https://huagongshe.com/reaction/423123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamateHCID 57750293—
ProductN-[3-amino-3-(4-chlorophenyl)propyl]methanesulfonamideHCID 5775032656.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

TFA (4 mL) was added to tert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamate (Intermediate 115) (275 mg, 0.76 mmol) and stirred at 20° C. for 2 hours. The reaction was vacuumed to dryness. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford N-(3-amino-3-(4-chlorophenyl)propyl)methanesulfonamide (113 mg, 56.7%) as a colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-b8a7f386d3a9466f8c20fb4b0c6f4d6e
Source noteuspto-grants-2012_01