反应 #6992

ord-422e54a7b8534818a58e13cc907fb18e

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Under N2 in a flame-dried 3-neck round bottomed flask fitted with a reflux condenser and magnetic stirrer
  2. 2
    其他while degassing with N2 for 5 min
  3. 3
    温度After heating at approximately 80° C. for 90 min.
  4. 4
    温度to 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
    其他The water layer was separated
  8. 8
    萃取extracted twice with EA
  9. 9
    洗涤washed with an aqueous solution of Rochelle salt (potassium sodium tartrate tetrahydrate)
  10. 10
    干燥The organic layer was dried with Na2SO4
  11. 11
    过滤filtered
  12. 12
    浓缩concentrated in vacuo to an oil
  13. 13
    其他chromatographed on a 15×5 cm column of silica gel
  14. 14
    洗涤eluting with CH2Cl2:hexanes (1:1)

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07084165B2uspto-grants-2006_08