Réaction #217977

ord-e4fb58fc619c4af0bb5cd54e96ad962f

Équation de réaction

CCOc1cc(C=O)ccc1O
3-ethoxy-4-hydroxy-benzaldehyde
N#Cc1ccc(Cl)nc1
6-chloro-nicotinonitrile
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOc1cc(C=O)ccc1Oc1ccc(C#N)cn1
title compound
Rendement 93.6%
CCOc1cc(C=O)ccc1Oc1ccc(C#N)cn1
6-(2-Ethoxy-4-formyl-phenoxy)-nicotinonitrile
Rendement 93.6%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreafter 3 h at 100° C. (no purification)

Mode opératoire

Using a method similar to Example 365, step 1, and using 3-ethoxy-4-hydroxy-benzaldehyde (3.00 g, 18.0 mmol), 6-chloro-nicotinonitrile (2.65 g, 18.0 mmol), and potassium carbonate (6.62 g, 45.2 mmol) in dimethylacetamide (90 mL), after 3 h at 100° C. (no purification) provides 4.52 g (93%) of the title compound as a yellow/white solid: mass spectrum (electrospray): m/z=269.0 (M+1); 1H NMR (CDCl3): 9.96 (s, 1H), 8.39 (d, 1H, J=2.0 Hz), 7.95 (dd, 1H, J=2.0, 8.3 Hz), 7.55-7.50 (m, 2H), 7.33 (d, 1H, J=7.8 Hz), 7.11 (d, 1H, J=9.3 Hz), 4.05 (q, 2H, J=6.8 Hz), 1.16 (t, 3H, J=6.8 Hz).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07381719B2uspto-grants-2008_06