Réaction #1106638

ord-4d0b3701ad2649e7bd7bd3f858fdd2fc

Équation de réaction

O=C(CO)c1ccccc1
2-hydroxyacetophenone
O=Cc1ccc(N2CCCCC2)nc1
6-(piperidin-1-yl)nicotinaldehyde
C[O][Na]
NaOCH3
O=C(C=Cc1ccccc1)c1ccccc1
chalcone
Rendement 43.5%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

1.72 g (12.6 mmol) of 2-hydroxyacetophenone, 2.0 g of 6-(piperidin-1-yl)nicotinaldehyde (10.5 mmol), and 10 ml of 25% wt NaOCH3 were reacted in 50 ml of dry THF to give 1.41 g (43.5%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 13.10 (s, 1H), 8.39 (d, J=2.4 Hz, 1H), 7.93-7.89 (m, 2H), 7.80 (d, d, J=2.4, 9.0 Hz), 7.51-7.42 (m, 2H), 7.03 (d, d, J=0.9, 8.4 Hz, 1H), 6.94 (d, d, d, J=1.2, 7.2, 8.1 Hz, 1H), 6.68 (d, J=9.0 Hz, 1H), 3.71-3.67 (m, 4H), 1.75-1.67 (m, 6H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08715761B2uspto-grants-2014_05