反应 #862

ord-84fae49193d148f395e8e28f50d554ab

反应方程式

N=C(N)NCCOCCO.O=C(O)CCC(=O)O
2-(2-hydroxyethoxy)ethylguanidine succinate
CC(=O)[O-]
acetate
CC(=O)OC(C)=O
acetic anhydride
CC(=O)OCCOCCNC(=N)N
title compound
收率 40.0%
CC(=O)OCCOCCNC(=N)N
2-(2-guanidinoethoxy)ethyl acetate
收率 40.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After the upper phase was removed by decantation
  2. 2
    其他the obtained crude product
  3. 3
    洗涤was washed five times with 50 ml of diethylether
  4. 4
    其他The product was purified by a silica gel column chromatography (eluent, chloroform/ethanol=2/1 containing 0.5% acetic acid)

实验过程

2.06 g (9.99 mmol) of 2-(2-hydroxyethoxy)ethylguanidine succinate, 8 ml of triethylamine, 0.122 mg (1.0 mmol) of 4-N,N-dimethylaminopyridine and 1.02 g (9.99 mmol) of acetic anhydride were placed in a 50 ml two neck flask and were stirred for 1 hour at room temperature. After the upper phase was removed by decantation, the obtained crude product was washed five times with 50 ml of diethylether. The product was purified by a silica gel column chromatography (eluent, chloroform/ethanol=2/1 containing 0.5% acetic acid) to obtain 1.00 g of the title compound (starch syrup-like, 4.0 mmol, 40.0% in yield) in the form of acetate. Results of the analysis of this compound are as follows.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723133uspto-grants-1998_03