Реакция #859

ord-0b3cb71fbde54da5a7c439131d7d2319

Уравнение реакции

CCNCCCOC
N-ethyl-3-methoxypropylamine
CC(=O)O
acetic acid
CC(=O)[O-]
acetate
N#CN
cyanamide
CCN(CCCOC)C(=N)N
title compound
Выход 50.0%
CCN(CCCOC)C(=N)N
N-3-methoxypropyl-N-ethylguanidine
Выход 50.0%

Реагенты

Нет

Растворители

Условия реакции

Температура
90°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter 12 hours of the reaction
  2. 2
    Другоеthe product was purified by a silica gel column chromatography (eluent, chloroform/ethanol=1/2 containing 0.5% acetic acid)

Методика

3.00 g (25.6 mmol) of N-ethyl-3-methoxypropylamine and 1.54 g (25.6 mmol) of acetic acid were placed in a 50 ml two neck flask. While heating the flask in a 90° C. oil bath, 1.08 g (25.6 mmol) of cyanamide was added. After 12 hours of the reaction, the product was purified by a silica gel column chromatography (eluent, chloroform/ethanol=1/2 containing 0.5% acetic acid) to obtain 2.80 g of the title compound (wax-like, 12.8 mmol, 50.0% in yield) in the form of acetate. Results of the analysis of this compound are as follows.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723133uspto-grants-1998_03