반응 #217965

ord-61fa8ecdafb44ee882ddcb421775cd98

반응 방정식

O
water
Cc1cc(C=O)ccc1O
4-hydroxy-3-methyl-benzaldehyde
N#Cc1ccc(Cl)nc1
6-chloro-nicotinonitrile
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cc(C=O)ccc1Oc1ccc(C#N)cn1
title compound
수율 89.4%
Cc1cc(C=O)ccc1Oc1ccc(C#N)cn1
6-(4-Formyl-2-methyl-phenoxy)-nicotinonitrile
수율 89.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONdilute
  2. 2
    추출extract with ethyl acetate (3×50 mL)
  3. 3
    세척Wash
  4. 4
    건조dry over anhydrous magnesium sulfate
  5. 5
    여과filter
  6. 6
    농축concentrate
  7. 7
    기타Purify the residue by silica gel chromatography (hexanes→ethyl acetate gradient/1.5 L)

실험 절차

Combine 4-hydroxy-3-methyl-benzaldehyde (0.502 g, 3.69 mmol), 6-chloro-nicotinonitrile (0.510 g, 3.68 mmol), and potassium carbonate (1.28 g, 9.26 mmol) in dimethylacetamide (18 mL) and warm to 100° C. After 1 h, cool to ambient temperature, dilute reaction mixture with water (40 mL), and extract with ethyl acetate (3×50 mL). Wash combined organic extracts with water and brine successively, dry over anhydrous magnesium sulfate, filter, and concentrate. Purify the residue by silica gel chromatography (hexanes→ethyl acetate gradient/1.5 L) to provide 0.784 g (89%) of the title compound as a light brown solid: mass spectrum (electrospray): m/z=239.0 (M+1);

출처

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