Réaction #487518

ord-c181300b85774c64a75f7795a498911c

Équation de réaction

O=c1ccc2ccc(O)cc2o1
7-hydroxycoumarin
[H-].[Na+]
NaH
C=CCCBr
4-bromo-1-butene
C=CCCOc1ccc2ccc(=O)oc2c1
4-(7-coumarinyloxy)-1-butene
Rendement 67.0%

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavageis washed with water (3×300 mL)
  2. 2
    AutreThe residue is chromatographed with the mixture (ethyl acetate-hexane)

Mode opératoire

A suspension of 7-hydroxycoumarin (3 g, 19.6 mmol) in DMF (20 ml) is treated with NaH (60% suspension in oil, 1.03 g, 25.9 mmol), then with 4-bromo-1-butene (2.65 g, 19.6 mmol). It is heated to 60° C. for 24 hours, then it is diluted with ethyl acetate (400 ml), and it is washed with water (3×300 mL) then with 1 M NaOH (3×200 ml). The residue is chromatographed with the mixture (ethyl acetate-hexane) to obtain 4-(7-coumarinyloxy)-1-butene (2.7 g, 67%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08741593B2uspto-grants-2014_06