Réaction #5145

ord-3c1df7ab18894dd9a67c2c7d77a2304e

Équation de réaction

C=C(C)C(=O)OCCOCCOCCOc1cccc([N+](=O)[O-])c1
compound ( 1-B )
C=C(C)C(=O)OCCOCCOCCOc1cccc([N+](=O)[O-])c1
2-(2-(2-(3-nitrophenoxy)ethoxy)ethoxy)ethyl methacrylate
[Cl-].[NH4+]
ammonium chloride
O
water
CC(C)O
isopropyl alcohol
C=C(C)C(=O)OCCOCCOCCOc1cccc(N)c1
2-(2-(2-(3-aminophenoxy)ethoxy)ethoxy)ethyl methacrylate

Conditions de réaction

Température
75°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter removing insoluble matters from the reaction mixture
  2. 2
    Filtrationby filtration, 200 ml of ethyl acetate and 500 ml of water
  3. 3
    workup.ADDITIONwere added to the reaction mixture
  4. 4
    Extractionthe ethyl acetate layer was extracted
  5. 5
    ConcentrationThe ethyl acetate layer was concentrated
  6. 6
    Autrethe residue was purified by silica gel column chromatography

Mode opératoire

A mixture of 25 g of reduced iron, 1 g of ammonium chloride, 50 ml of water, and 250 ml of isopropyl alcohol was raised to a temperature of 75° C. with stirring and after adding dropwise an ethyl acetate solution of the compound (1-B) to the aqueous solution (the mixture) over a period of one hour, the resultant mixture was further stirred for 2 hours. After removing insoluble matters from the reaction mixture by filtration, 200 ml of ethyl acetate and 500 ml of water were added to the reaction mixture and the ethyl acetate layer was extracted. The ethyl acetate layer was concentrated and the residue was purified by silica gel column chromatography using chloroform as a developing solvent to provide 15.3 g of 2-(2-(2-(3-aminophenoxy)ethoxy)ethoxy)ethyl methacrylate (1-C).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05243004uspto-grants-1993_09