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Methanol → Heptyl 4,4-dinitropentanoate

HRID 573473
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 573473
[N+:1]([CH:4]([N+:6]([O-:8])=[O:7])[CH3:5])([O-:3])=[O:2].[OH-].[K+].[C:11]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])(=[O:14])[CH:12]=[CH2:13].CO>O>[N+:1]([C:4]([N+:6]([O-:8])=[O:7])([CH3:5])[CH2:13][CH2:12][C:11]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[O:14])([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 887MethanolHCID 14797Potassium HydroxideHCID 17257Heptyl acrylateHCID 611501,1-Dinitroethane

Produkt 1

HCID 86717672Heptyl 4,4-dinitropentanoateAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962Water
Lösungsmittel
2×

Versuchsvorschrift

Dinitroethane (2.4 g, 0.02 mol) and potassium hydroxide (1.2 g, 0.22 mol) were dissolved in 50 mL of water to form a first solution. 50 mL of water was added to the first solution to dissolve a salt remaining in the first solution to form a second solution. Heptyl acrylate (9.5 mL, 0.05 mol) was mixed with 50 mL of methanol, and then the mixture was slowly added to the second solution to form a third solution. The third solution was stirred at room temperature for 3 hours. The reaction product was extracted by diethyl ether, and was then distilled under reduced pressure to obtain yellow liquid heptyl 4,4-dinitropentanoate (4.8 g, yield: 83%).

Aufarbeitung

  1. customto form a first solution
  2. dissolutionto dissolve a salt
  3. customto form a second solution
  4. additionthe mixture was slowly added to the second solution
  5. customto form a third solution
  6. extractionThe reaction product was extracted by diethyl ether
  7. distillationwas then distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-97abad4e7d064781ae05e48e586e3e14
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09029591B2

Notizen zur Reaktion

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