반응 #985257

ord-6f616e102d984141acf2882765e3dfaa

반응 방정식

O=[N+]([O-])c1ccc(/C=C/c2nc3ccccc3s2)cc1
2-(4-nitrophenylethenyl)benthiazole
O=[N+]([O-])c1ccc(/C=C/c2nc3ccccc3s2)cc1
Trans-2-(4-Nitrophenylethenyl)benzothiazole
O.O.[Cl][Sn][Cl]
tin (II) chloride dihydrate
Nc1ccc(C=Cc2nc3ccccc3s2)cc1
product 12
수율 9.3%
Nc1ccc(C=Cc2nc3ccccc3s2)cc1
2-(4-Aminophenylethenyl)benzothiazole
수율 9.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was refluxed under N2 for 4 hrs
  2. 2
    기타Ethanol was removed by vacuum evaporation
  3. 3
    workup.DISSOLUTIONThe residue was dissolved into ethyl acetate (20 ml)
  4. 4
    세척washed with NaOH solution (1 N, 3×20 ml) and water (3×20 ml)
  5. 5
    건조dried over MgSO4
  6. 6
    기타Evaporation to dryness

실험 절차

A mixture of 2-(4-nitrophenylethenyl)benthiazole 11 (500 mg, 1.7 mmol) and tin (II) chloride dihydrate (1.18 g, 5.2 mmol) in anhydrous ethanol (20 ml) was refluxed under N2 for 4 hrs. Ethanol was removed by vacuum evaporation. The residue was dissolved into ethyl acetate (20 ml), washed with NaOH solution (1 N, 3×20 ml) and water (3×20 ml), and dried over MgSO4. Evaporation to dryness gave 40 mg (8.0%) of product 12.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07351401B2uspto-grants-2008_04