Cyclopropanecarboxylic acid → HCID 178526476, Verbindung

HRID 19744

Reaktionsgleichung

Reaktionsgleichung von HRID 19744
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([NH2:11])[CH:5]=1)([O-:3])=[O:2].[CH:12]1([C:15](O)=O)[CH2:14][CH2:13]1>>[CH:12]1([C:15]2[NH:10][C:7]3[CH:8]=[CH:9][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][C:6]=3[N:11]=2)[CH2:14][CH2:13]1

Komponenten

3

Edukt 2

HCID 15655Cyclopropanecarboxylic acidHCID 51117914-Nitro-1,2-phenylenediamine

Produkt 1

HCID 178526476HCID 178526476, VerbindungAusbeute 98 %

Versuchsvorschrift

By analogy with a described method (WO 96/04270), a solution of 5 g (32.65 mmol) of 4-nitro-1,2-phenylenediamine in 77 ml (0.979 mol) of cyclopropanecarboxylic acid is stirred at reflux for 14 hours. The reaction mixture is then concentrated under reduced pressure and taken up in 150 ml of ethyl acetate and 100 ml of sodium hydrogen carbonate. The organic phase is washed with 100 ml of water and then with 50 ml of saturated sodium chloride solution, dried over magnesium sulfate and then concentrated under reduced pressure. 6.5 g of a brown oil are obtained, and are used without further purification in the following step.

Aufarbeitung

  1. temperatureat reflux for 14 hours
  2. concentrationThe reaction mixture is then concentrated under reduced pressure
  3. washThe organic phase is washed with 100 ml of water
  4. dry with materialwith 50 ml of saturated sodium chloride solution, dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-4b30a245a00a456e92a94bd884845186
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07745467B2

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