반응 #6992

ord-422e54a7b8534818a58e13cc907fb18e

반응 방정식

O=Cc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde
CN(C)C=O
DMF
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
title product
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
5-CYANO-2-(3,4-DICHLOROPHENOXY)-BENZALDEHYDE

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Under N2 in a flame-dried 3-neck round bottomed flask fitted with a reflux condenser and magnetic stirrer
  2. 2
    기타while degassing with N2 for 5 min
  3. 3
    온도After heating at approximately 80° C. for 90 min.
  4. 4
    온도to cool to room temperature
  5. 5
    workup.ADDITIONThe reaction mixture was then diluted with water and ethyl acetate (EA)
  6. 6
    workup.STIRRINGstirred another 10 min
  7. 7
    기타The water layer was separated
  8. 8
    추출extracted twice with EA
  9. 9
    세척washed with an aqueous solution of Rochelle salt (potassium sodium tartrate tetrahydrate)
  10. 10
    건조The organic layer was dried with Na2SO4
  11. 11
    여과filtered
  12. 12
    농축concentrated in vacuo to an oil
  13. 13
    기타chromatographed on a 15×5 cm column of silica gel
  14. 14
    세척eluting with CH2Cl2:hexanes (1:1)

실험 절차

Under N2 in a flame-dried 3-neck round bottomed flask fitted with a reflux condenser and magnetic stirrer, a mixture of 5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde (3.0 g, 8.7 mmol), zinc (II) cyanide (1.5 g, 13 mmol) and tetrakis(triphenylphosphine)palladium (0) (1.5 g, 1.3 mmol) in anhydrous DMF (145 ml) was stirred at room temperature while degassing with N2 for 5 min. After heating at approximately 80° C. for 90 min., the reaction was judged complete by thin layer chromatography (50% CH2Cl2:hexanes) and was allowed to cool to room temperature. The reaction mixture was then diluted with water and ethyl acetate (EA) and stirred another 10 min. The water layer was separated, extracted twice with EA and combined with the original EA layer, and washed with an aqueous solution of Rochelle salt (potassium sodium tartrate tetrahydrate) followed by aqueous NaCl. The organic layer was dried with Na2SO4, filtered and concentrated in vacuo to an oil. The oil was flash chromatographed on a 15×5 cm column of silica gel, eluting with CH2Cl2:hexanes (1:1) to obtain the title product as a white solid, 1.5 g (60%), m.p. 122–126° C.

출처

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