반응 #929

ord-9c0049ffd5bd4c2597bd8dc1da4f9125

반응 방정식

N#Cc1c([N+](=O)[O-])cccc1[N+](=O)[O-]
2,6-dinitrobenzonitrile
Sc1ccccc1
thiophenol
O=C([O-])[O-].[K+].[K+]
K2CO3
c1ccncc1
Pyridine
N#Cc1c(Sc2ccccc2)cccc1[N+](=O)[O-]
2-nitro-6-(phenylthio)benzonitrile
수율 89.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The yellow precipitate was collected by filtration
  2. 2
    세척washed with 1N NaOH, water
  3. 3
    기타dried

실험 절차

An ice water bath-cooled mixture of 2.0 g (0.01 mol) of 2,6-dinitrobenzonitrile (Lancaster Synthesis, Inc., Windham, N.H. 03087), 1.06 ml (0.01 mol) of thiophenol, and 1.44 g (0.01 mol) of anhydrous K2CO3 in 50 mL of DMF was stirred for 0.5 h. Pyridine was added to the reaction mixture until it became basic, and was followed by the addition of approximately 100 mL of H2O. The yellow precipitate was collected by filtration, washed with 1N NaOH, water and dried to give 1.94 g (89%) of 2-nitro-6-(phenylthio)benzonitrile as a yellow solid: mp 106°-107° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723452uspto-grants-1998_03