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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708326Generated: October 30, 2026

Trimethylamine → N,N,N-Trimethyl-2-oxo-2-(prop-2-yn-1-ylamino)ethanaminium bromide

https://huagongshe.com/reaction/708326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
Reactant2-bromo-N-(prop-2-yn-1-yl)acetamideHCID 11159617—
SolventAcetonitrileHCID 6342—
ProductN,N,N-Trimethyl-2-oxo-2-(prop-2-yn-1-ylamino)ethanaminium bromideHCID 11837991197%

Reaction Steps

To a solution of 2-bromo-N-(prop-2-yn-1-yl)acetamide (0.6 g, 3.4 mmol) in acetonitrile (5 mL) was added trimethylamine (30% in MeOH, 5 mL). The mixture was stirred at room temperature for 16 h and concentrated in vacuo. The resulting residue was triturated with ether, resulting in the title compound (780 mg, 97%); LCMS: m/z=155.1 (M+1); 1H NMR (300 MHz, DMSO-d6) δ 9.03 (t, J=5.3 Hz, 1H), 4.17 (s, 2H), 3.95 (dd, J=5.4, 2.6 Hz, 2H), 3.23 (s, 9H), 2.09 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-8b2364f852df41e5ae0cdc996b161d10
Source noteuspto-grants-2015_11