Reaktion #487505

ord-05501bd9f7d0469489ae764d524d12f8

Reaktionsgleichung

COC(=O)CCCC#CCO
( 30 )
COC(=O)CCCC#CCO
7-Hydroxy-hept-5-ynoic acid methyl ester
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
c1c[nH]cn1
imidazole
II
iodine
COC(=O)CCCC#CCI
propargyl iodide
Ausbeute 83.0%
COC(=O)CCCC#CCI
7-Iodo-hept-5-ynoic acid methyl ester
Ausbeute 83.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenrinsing with 5 mL dichloromethane
  2. 2
    Sonstigethe dichloromethane was evaporated in vacuo to about 2 mL
  3. 3
    Filtrationthe resulting mixture filtered through basic alumina
  4. 4
    Waschenwashing with 10% ethyl acetate/hexanes
  5. 5
    SonstigePurification by flash chromatography on silica gel (10% ethyl acetate/hexanes)

Vorschrift

A solution of (30) (1.347 g, 8.6 mmol) in 5 mL dichloromethane was added to a mixture of triphenylphosphine (2.725 g, 10.4 mmol), imidazole (726 mg, 10.7 mmol), and iodine (2.602 g, 10.3 mmol) in 34 mL dichloromethane, rinsing with 5 mL dichloromethane. After 40 minutes, the dichloromethane was evaporated in vacuo to about 2 mL and the resulting mixture filtered through basic alumina, washing with 10% ethyl acetate/hexanes. Purification by flash chromatography on silica gel (10% ethyl acetate/hexanes) gave 1.878 g (7.1 mmol, 83%) of the propargyl iodide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08741281B2uspto-grants-2014_06