Réaction #59568

ord-23465df4dcd94ce797be335283abd1be

Équation de réaction

O=C1CC(c2cccc(F)c2)Oc2ccc(O)cc21
2-(3-fluorophenyl)-6-hydroxychroman-4-one
CC(=O)c1cc(O)ccc1O
2′,5′-dihydroxyacetophenone
O=Cc1ccc(F)cc1
4-fluorobenzaldehyde
O=C1CC(c2ccc(F)cc2)Oc2ccc(O)cc21
6-Hydroxy-2-(4-fluorophenyl)chroman-4-one

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe product was recrystallised from acetic acid

Mode opératoire

6-Hydroxy-2-(4-fluorophenyl)chroman-4-one was prepared as described for 2-(3-fluorophenyl)-6-hydroxychroman-4-one in Example 9(a) starting from 2.0 g of 2′,5′-dihydroxyacetophenone and 1.6 ml of 4-fluorobenzaldehyde. The product was recrystallised from acetic acid. 1H NMR (400 MHz, d6-DMSO) δ: 7.59 (m, 2H), 7.27 (m, 2H), 7.14 (d, 1H, J 3.1 Hz), 7.05 (dd, 1H, J 8.9, 3.1 Hz), 6.96 (d, 1H, J 8.9 Hz), 5.56 (dd, 1H, J 13.2, 2.8 Hz), 3.18 (dd, 1H, J-16.9, 13.2 Hz), 2.77 (dd, 1H, J −16.9, 2.8 Hz).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07425568B2uspto-grants-2008_09