Реакция #795508

ord-8b2364f852df41e5ae0cdc996b161d10

Уравнение реакции

C#CCNC(=O)CBr
2-bromo-N-(prop-2-yn-1-yl)acetamide
CN(C)C
trimethylamine
C#CCNC(=O)C[N+](C)(C)C.[Br-]
title compound
Выход 97.0%
C#CCNC(=O)C[N+](C)(C)C.[Br-]
N,N,N-Trimethyl-2-oxo-2-(prop-2-yn-1-ylamino)ethanaminium bromide
Выход 97.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated in vacuo
  2. 2
    ДругоеThe resulting residue was triturated with ether

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09174978B2uspto-grants-2015_11