HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650824Generated: October 26, 2026
Trifluoroacetic acid → N-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamide
https://huagongshe.com/reaction/650824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamic acid tert-butyl ester | HCID 20677519 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamide | HCID 10561338 | 51.9% |
Reaction Steps
At 0° C., trifluoroacetic acid (6 ml) was added to a solution of N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamic acid tert-butyl ester (870 mg, 2.6 mmol) in dichloromethane (6 ml). The reaction mixture was stirred for 50 min. Dichloromethane (24 ml) was added. A saturated aqueous solution of sodium hydrogen carbonate (34 ml) was added. Solid sodium hydrogen carbonate was added, until pH 7 was obtained. The phases were separated. The aqueous phase was extracted with dichloromethane (3×50 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash crhomatography on silica (60 g), using dichloromethane/methanol/25% aqueous ammonia (100:10:1) as eluent to give 308 mg of N-(2-(2-(methylamino)ethyl)phenyl)methanesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274584B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-7728c890650447bdbdef7479c615b0c3 |
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| Source note | uspto-grants-2001_08 |
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