StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Hydrochloric Acid → 1-Chlorononan-4-one

HRID 26593
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 26593
[CH2:1](Br)[CH2:2][CH2:3][CH2:4][CH3:5].[Mg].[Cl:8][CH2:9][CH2:10][CH2:11][C:12]#N.Cl.CC[O:17]CC>>[Cl:8][CH2:9][CH2:10][CH2:11][C:12](=[O:17])[CH2:1][CH2:2][CH2:3][CH2:4][CH3:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 80571-BromopentaneHCID 123364-ChlorobutyronitrileHCID 5462224Magnesium

Produkt 1

HCID 203861031-Chlorononan-4-one

Versuchsvorschrift

To the Grignard reagent prepared from a mixture of amyl bromide (226.59 g.; 1.5 moles) and magnesium (36.48 g.; 1.5 moles) in ether (1000 ml.) is added, dropwise, during one hour, 4-chlorobutyronitrile (155.34 g.; 1.5 moles). Stirring is continued for an additional one hour. The reaction mixture is poured into a mixture of finely crushed ice (1000 g.) and concentrated hydrochloric acid (750 ml.). The ether layer is separated quickly and discarded. The aqueous layer is heated on a steam bath for one hour to hydrolyze the intermediate imine and cause the separation of the ketone as an oil. After cooling, the oil is extracted with ether and the combined extracts are washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is removed under vacuum and the residual oil is distilled to give 69.0 g. (26%) of colorless oil, b.p. 115°-117° C./14 mm.; pmr (CDCl3) δ0.090 (3H,t), 3.56 (2H,t,CH2Cl).

Aufarbeitung

  1. additionis added
  2. waitis continued for an additional one hour
  3. customThe ether layer is separated quickly
  4. temperatureThe aqueous layer is heated on a steam bath for one hour
  5. customthe separation of the ketone as an oil
  6. temperatureAfter cooling
  7. extractionthe oil is extracted with ether
  8. washthe combined extracts are washed with saturated sodium chloride solution
  9. dry with materialdried over anhydrous sodium sulfate
  10. customThe solvent is removed under vacuum
  11. distillationthe residual oil is distilled
  12. customto give 69.0 g

Quellen und Nachweise

ORD-Eintrag
ord-2fa940aaf71b4ebab38dfed93ca83285
Quelldatensatz
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04150235

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion