Reaktion #861

ord-64d5f5dd2f664288acccc0452c5aa2a9

Reaktionsgleichung

NCCOCCOC(=O)c1ccccc1
2-(2-aminoethoxy)ethyl benzoate
CC(=O)O
acetic acid
CC(=O)[O-]
acetate
N#CN
cyanamide
N=C(N)NCCOCCOC(=O)c1ccccc1
title compound
Ausbeute 62.1%
N=C(N)NCCOCCOC(=O)c1ccccc1
2-(2-guanidinoethoxy)ethyl benzoate
Ausbeute 62.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter 6 hours of the reaction
  2. 2
    Sonstigethe product was purified by a silica gel column chromatography (eluent, chloroform/ethanol=1/2 containing 0.5% acetic acid)

Vorschrift

2.14 g (10.2 mmol) of 2-(2-aminoethoxy)ethyl benzoate and 0.624 g (10.4 mmol) of acetic acid were placed in a 50 ml two neck flask. While heating the flask in a 90° C. oil bath, 0.680 g (16.2 mmol) of cyanamide was added. After 6 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 1.97 g of the title compound (wax-like, 6.33 mmol, 62.0% in yield) in the form of acetate. Results of the analysis of this compound are as follows.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723133uspto-grants-1998_03