반응 #217904

ord-e6711d9e40a94a29adc61f2855fa4077

반응 방정식

O
water
Cc1cc(C=O)ccc1O
4-hydroxy-3-methyl-benzaldehyde
O=C([O-])[O-].[K+].[K+]
K2CO3
N#Cc1ccc(Cl)nc1
6-chloronicotinonitrile
Cc1cc(C=O)ccc1Oc1ccc(C#N)cn1
title compound
수율 97.1%
Cc1cc(C=O)ccc1Oc1ccc(C#N)cn1
6-(4-Formyl-2-methyl-phenoxy)-nicotinonitrile
수율 97.1%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출Extract the aqueous layer with EtOAc
  2. 2
    건조Dry the organic layer over Na2SO4
  3. 3
    기타Dry under vacuum at 45° C. overnight

실험 절차

Combine 4-hydroxy-3-methyl-benzaldehyde (401 mg, 2.94 mmol), K2CO3 (570 mg, 4.12 mmol) and 6-chloronicotinonitrile (408 mg, 2.94 mmol) in DMF (6 ml), heat at 100° C. After 4 h cool to ambient temperature and pour into water. Extract the aqueous layer with EtOAc. Dry the organic layer over Na2SO4 and eliminate the solvent. Dry under vacuum at 45° C. overnight to get the title compound (680 mg, 97%). 1H-NMR (CDCl3, 400 MHz): 9.99 (s, 1H), 8.43 (d, 1H, J=2.5 Hz), 7.97 (dd, 1H, J=2.5 and 8.8 Hz), 7.84 (bs, 1H), 7.80 (dd, 1H, J=2.5 and 8.8 Hz), 7.22 (d, 1H, J=8.4 Hz), 7.11 (d, 1H, J=8.4 Hz), 2.24 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07381719B2uspto-grants-2008_06