Reaktion #1693

ord-69104add2a2849aba17decff43b8a344

Reaktionsgleichung

N#Cc1ccc(CO)s1
2-cyano-5-(hydroxymethyl)thiophene
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrC(Br)(Br)Br
carbon tetrabromide
N#Cc1ccc(CBr)s1
2-cyano-5-(bromomethyl)thiophene
Ausbeute 75.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent was removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in chloroform
  3. 3
    WaschenThe product was eluted
  4. 4
    workup.ADDITIONFractions containing pure product (as judged by TLC)
  5. 5
    Einengenconcentrated in vacuo

Vorschrift

To a solution of 2-cyano-5-(hydroxymethyl)thiophene (6.0 g, 43 mmol) in THF (50 mL) was added triphenylphosphine (15.7 g, 47 mmol) and carbon tetrabromide (12.3 g, 47 mmol). After stirring overnight under nitrogen atmosphere at room temperature, the solvent was removed in vacuo and the residue was dissolved in chloroform, then adsorbed onto silica gel and loaded onto a silica gel column. The product was eluted using an ethyl acetate/hexanes gradient. Fractions containing pure product (as judged by TLC) were pooled and concentrated in vacuo to give 6.5 g (75%) of 2-cyano-5-(bromomethyl)thiophene.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726159uspto-grants-1998_03