반응 #722735

ord-605fdc7c832c43279cd877d18b16064c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06187955B1uspto-grants-2001_02