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Hydrochloric Acid → HCID 85826896, Verbindung

HRID 1254957
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1254957
[C:1](OC)(=[O:3])C.[C:6](#[N:14])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[ClH:15].CC1CCCCC1>CO>[ClH:15].[C:6](=[NH:14])([O:3][CH3:1])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 6584Methyl AcetateHCID 7962MethylcyclohexaneHCID 31286Octanenitrile

Produkt 1

HCID 85826896HCID 85826896, VerbindungAusbeute 93,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Methanol (2.81 g) and methyl acetate (30 ml) were added to octanenitrile (10.00 g), and the mixture was cooled to 0° C. Hydrogen chloride (7.50 g) was added and the mixture was stirred for 25 hours at the same temperature. Methylcyclohexane (60 ml) was added to the reaction solution, and then the solvent was distilled off under reduced pressure. Methylcyclohexane (20 ml) was added to the residue, the mixture was stirred for 1.5 hours at room temperature, and then crystals were filtered. The crystals were washed with methylcyclohexane and dried under reduced pressure to give the title compound as a white solid (14.45 g, 93.4% yield).

Aufarbeitung

  1. distillationthe solvent was distilled off under reduced pressure
  2. additionMethylcyclohexane (20 ml) was added to the residue
  3. stirringthe mixture was stirred for 1.5 hours at room temperature
  4. filtrationcrystals were filtered
  5. washThe crystals were washed with methylcyclohexane
  6. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ea6a390f11f543fbae7d591a621f148f
Quelldatensatz
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08455659B2

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