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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713899Generated: October 30, 2026

Trifluoroacetic acid → 3-amino-N-(methylsulfonyl)propanamide

https://huagongshe.com/reaction/713899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 3-(methylsulfonamido)-3-oxopropylcarbamateHCID 86668418—
SolventDichloromethaneHCID 6344—
Product3-amino-N-(methylsulfonyl)propanamideHCID 1402823580%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-butyl 3-(methylsulfonamido)-3-oxopropylcarbamate (3.6 g, 15.1 mmol) was dissolved in DCM (60 mL). Then CF3COOH (1.1 mL, 0.3 mmol, 20 equiv) was added to the mixture at 0° C. and stirred for 2 h at 0° C. The reaction mixture was concentrated. The residue was purified by flash chromatography to give 3-amino-N-(methylsulfonyl)propanamide as a transparent solid (1.8 g, 80%), (mobile phase: CH3OH/H2O=0˜5%). ESI-MS (M+1)+: 167.0. 1H NMR (400 MHz, CD3OD) δ: 3.21˜3.11 (m, 2H), 3.07 (s, 3H), 2.60˜2.54 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-fca08ac47c7c488f877f357dfc8e259f
Source noteuspto-grants-2015_11