تفاعل #862

ord-84fae49193d148f395e8e28f50d554ab

معادلة التفاعل

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
المردود 40.0%
CC(=O)OCCOCCNC(=N)N
2-(2-guanidinoethoxy)ethyl acetate
المردود 40.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723133uspto-grants-1998_03