반응 #6996

ord-d3006829c64043e1abcf88cb05d868f9

반응 방정식

O=Cc1cc(F)ccc1Oc1ccc(Cl)c(Cl)c1
2-(3,4-dichloro-phenoxy)-5-fluorobenzaldehyde
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
O=C(O)c1cc(F)ccc1Oc1ccc(Cl)c(Cl)c1
2-(3,4-dichlorophenoxy)-5-fluoro-benzoic acid

용매

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the reaction was quenched with 8 mL of isopropanol
  2. 2
    여과filtered through a pad of d.e
  3. 3
    농축The filtrate was concentrated in vacuo to approximately ¼ volume
  4. 4
    workup.ADDITIONdiluted with water
  5. 5
    추출extracted several times with CHCl3
  6. 6
    세척The organic layers were washed with water
  7. 7
    건조with saturated NaCl and finally dried over MgSO4
  8. 8
    농축concentrated

실험 절차

Alternatively, a solution of 4.28 g (15 mmol) of 2-(3,4-dichloro-phenoxy)-5-fluorobenzaldehyde (Preparation no. 5) in 25 mL of acetone was cooled to 5–10° C. and treated via syringe with 5.8 mL (15.6 mmol) of 2.67 M Jones reagent*. After 1 hr at this temperature, the reaction was quenched with 8 mL of isopropanol, allowed to warm to 25° C., and filtered through a pad of d.e. The filtrate was concentrated in vacuo to approximately ¼ volume, diluted with water and extracted several times with CHCl3. The organic layers were washed with water, then with saturated NaCl and finally dried over MgSO4 and concentrated to provide 2-(3,4-dichlorophenoxy)-5-fluoro-benzoic acid as a tan solid, 4.19 g. 1H-nmr (CDCl3, 400 MHz, δ): 7.78 (dd, 1H), 7.38 (d, 1H), 7.27 (m, 1H), 6.98 (m, 2H), 6.81 (dd, 1H). *Jones reagent was prepared from 13.4 g of chromium trioxide and 11.5 mL of concentrated H2SO4, diluted to a final volume of 50 mL with H2O.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07084165B2uspto-grants-2006_08