Réaction #577219

ord-64c126458c8142878265339f4570ce1d

Équation de réaction

C=CCBr
3-Bromo-1-propene
Cc1cc(=O)oc2cc(O)ccc12
7-hydroxy-4-methylcoumarin
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C=CCOc1ccc2c(C)cc(=O)oc2c1
2
Rendement 96.2%
C=CCOc1ccc2c(C)cc(=O)oc2c1
7-Allyloxy-4-methylcoumarin
Rendement 96.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe resulting mixture was then refluxed for 4 h
  2. 2
    Températureto cool
  3. 3
    Filtrationthe K2CO3 filtered off
  4. 4
    Lavagewashed with fresh acetone
  5. 5
    AutreThe solvent was removed in vacuo
  6. 6
    Autrethe residue was crystallized from methanol

Mode opératoire

3-Bromo-1-propene (2.95 mL, 34.06 mmol) was added dropwise under argon to a stirred mixture of 7-hydroxy-4-methylcoumarin 1 (2.0 g, 11.35 mmol) and anhydrous potassium carbonate (K2CO3) (2.35 g, 17.03 mmol) in acetone (50 mL). The resulting mixture was then refluxed for 4 h, after which it was allowed to cool, and the K2CO3 filtered off and washed with fresh acetone. The solvent was removed in vacuo and the residue was crystallized from methanol to afford 2 as white-cream crystals (2.36 g, 96%). TLC (hexane/ethyl acetate, 1:3): Rf=0.63. mp 110° C. 1H NMR (CDCl3, 500 MHz) δ 2.39 (s, 3H, CH3), 4.60 (d, J=5.0 Hz, 2H, CH2), 5.33 (d, J=10.5 Hz, 1H), 5.44 (d, J=17.5 Hz, 1H), 6.05 (m, 1H), 6.12 (s, 1H), 6.80 (s, 1H), 6.87 (dd, J=1.5, 9.0 Hz, 1H), 7.49 (d, J=9.0 Hz, 1H). 13C NMR (CDCl3, 125 MHz) δ 18.70, 69.29, 101.84, 112.05, 112.79, 113.75, 118.51, 125.64, 132.31, 152.61, 152.26, 161.26, 161.65. ESIMS calcd for C13H13O3 [M+H]+ 217.1, found 217.1.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07527934B2uspto-grants-2009_05