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

Chloroacetonitrile → 2-(4-oxopiperidin-1-yl)acetonitrile

HRID 1058610
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1058610
O.Cl.[NH:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1.Cl[CH2:11][C:12]#[N:13].C(N(C(C)C)CC)(C)C>O1CCCC1>[O:9]=[C:6]1[CH2:7][CH2:8][N:3]([CH2:11][C:12]#[N:13])[CH2:4][CH2:5]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 7856ChloroacetonitrileHCID 81531DiisopropylethylamineHCID 2723901Piperonylamine

Produkt 1

HCID 27609212-(4-oxopiperidin-1-yl)acetonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A suspension of 25.0 g of 4-piperidinone monohydrochloride monohydrate, 11.5 ml of chloroacetonitrile and 57.0 ml of diisopropylethylamine in 250 ml of tetrahydrofuran was refluxed for 10 hours. After the reaction, an insoluble matter was filtered off. The filtrate was added with saturated aqueous sodium hydrogencarbonate solution and extracted with a mixture of ethyl acetate and methanol (10:1). The extract was dried, and the solvent was evaporated to give brown crystals. The crystals were washed with a mixture of ethyl acetate and n-heptane to give 15.7 g of pale brown crystals.

Aufarbeitung

  1. temperaturewas refluxed for 10 hours
  2. customAfter the reaction
  3. filtrationan insoluble matter was filtered off
  4. additionThe filtrate was added with saturated aqueous sodium hydrogencarbonate solution
  5. extractionextracted with a mixture of ethyl acetate and methanol (10:1)
  6. customThe extract was dried
  7. customthe solvent was evaporated
  8. customto give brown crystals
  9. washThe crystals were washed with a mixture of ethyl acetate and n-heptane

Quellen und Nachweise

ORD-Eintrag
ord-d96a4e9b8c024403a4170b9d176b4a83
Quelldatensatz
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06518265B1

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion