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Pyridine → n-Pentyltriflate

HRID 1944513
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1944513
N1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)CCCC.[S:13]([O:20]S(C(F)(F)F)(=O)=O)([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14]>>[CH2:2]([O:20][S:13]([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14])[CH2:3][CH2:4][CH2:5][CH3:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1049PyridineHCID 62761-PentanolHCID 67749Trifluoromethanesulfonic anhydride

Produkt 1

HCID 10987782n-Pentyltriflate

Versuchsvorschrift

To a nitrogen flushed round bottom flask equipped with a stir bar was added pyridine (0.81 mL, 10.0 mmol) and n-pentanol (1.09 mL, 10.0 mmol). The reaction was cooled in an ice bath and triflic anhydride (1.69 mL, 10.0 mmol) was added dropwise. The ice bath was allowed to melt over two hours at which time the entire reaction mixture was filtered over a column of silica gel eluting with dichloromethane. The filtrate was carefully evaporated in vacuo then carried on without further purification(1.11 g, 5.04 mmol).

Aufarbeitung

  1. custom
To a nitrogen flushed round bottom flask equipped with a stir bar
  • temperatureThe reaction was cooled in an ice bath
  • customthe entire reaction mixture
  • filtrationwas filtered over a column of silica gel eluting with dichloromethane
  • customThe filtrate was carefully evaporated in vacuo
  • customthen carried on without further purification(1.11 g, 5.04 mmol)
  • Quellen und Nachweise

    ORD-Eintrag
    ord-905ce1a5152a4b5a9c957a0b8bbd92f8
    Quelldatensatz
    uspto-grants-2013_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US08394828B2

    Notizen zur Reaktion

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