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

Diethyl (cyanomethyl)phosphonate → HCID 67451464, Verbindung

HRID 1853064
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1853064
[C:1]([CH2:3]P(=O)(OCC)OCC)#[N:2].CC(C)([O-])C.[K+].[F:18][C:19]1([F:24])[CH2:21][CH:20]1[CH:22]=O>C1COCC1>[F:18][C:19]1([F:24])[CH2:21][CH:20]1[CH:22]=[CH:3][C:1]#[N:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 75676Diethyl (cyanomethyl)phosphonateHCID 206984562,2-Difluorocyclopropane-1-carbaldehydeHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 67451464HCID 67451464, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of diethyl cyanomethylphosphonate (4.09 g; 23.1 mmol) in dry THF (200 mL) at 0° C. under nitrogen was added potassium t-butoxide (23.1 mmol; 1M solution in THF). The mixture was stirred for 1 hour. The solution of 2,2-difluorocyclopropanecarbaldehyde from Step A was added and the mixture was stirred while allowing to warm to ambient temperature. A portion of the solvent was removed under reduced pressure and the remaining solution was diluted with ammonium chloride solution (50 mL). The mixture was extracted into ethyl acetate (2×50 mL). The combined extracts were dried (magnesium sulfate and sodium sulfate), filtered and evaporated under reduced pressure. The material was purified by chromatography on silica gel, eluting with hexane/ethyl acetate (3:1) to give 3-(2,2-difluorocyclopropyl)acrylonitrile (0.50 g) as a pale yellow oil (containing some ethyl acetate).

Aufarbeitung

  1. stirringthe mixture was stirred
  2. customA portion of the solvent was removed under reduced pressure
  3. additionthe remaining solution was diluted with ammonium chloride solution (50 mL)
  4. extractionThe mixture was extracted into ethyl acetate (2×50 mL)
  5. dry with materialThe combined extracts were dried (magnesium sulfate and sodium sulfate)
  6. filtrationfiltered
  7. customevaporated under reduced pressure
  8. customThe material was purified by chromatography on silica gel
  9. washeluting with hexane/ethyl acetate (3:1)

Quellen und Nachweise

ORD-Eintrag
ord-ab1f4c180f45419590f13cc6e90e8de6
Quelldatensatz
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08962596B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion