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Hexanal → Oct-2-enenitrile

HRID 1505475
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1505475
CC(C)([O-])C.[K+].[C:7]([CH2:9]P(=O)(OCC)OCC)#[N:8].[CH:18](=O)[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>O1CCCC1>[C:7](#[N:8])[CH:9]=[CH:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6184HexanalHCID 75676Diethyl (cyanomethyl)phosphonateHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 54249989Oct-2-enenitrileAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Versuchsvorschrift

To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (165 mL, 0.165 mol) at 0° C. was added dropwise a solution of diethyl cyanomethylphosphonate (27 mL, 0.17 mol) in tetrahydrofuran (100 mL). The reaction was warmed to room temperature and then cooled to 0° C. again after stirring for 30 min. To the reaction mixture was added a solution of hexanal (18 mL, 0.15 mol) in tetrahydrofuran (150 mL). The reaction was stirred overnight, allowed to warm up to room temperature. The reaction was quenched with water and extracted with ethyl acetate (EtOAc). The combined organic layers were washed with brine, dried over MgSO4, concentrated, and purified on silica gel (eluting with 0 to 15% EtOAc in hexanes) to provide the desired product (˜17 g, 92%) as a mixture of cis and trans isomers. MS calculated for C8H14N(M+H)+: m/z=124.113. Found: 124.3.

Aufarbeitung

  1. temperaturecooled to 0° C. again
  2. stirringThe reaction was stirred overnight
  3. temperatureto warm up to room temperature
  4. customThe reaction was quenched with water
  5. extractionextracted with ethyl acetate (EtOAc)
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. custompurified on silica gel (eluting with 0 to 15% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-97c03f637e2947eda8a8ed996b3ffded
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09216984B2

Notizen zur Reaktion

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