2-benzylsulfanylaniline

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(amino)thiophenol and 2-(methylthio)aniline were purchased from Aldrich Chemical Company.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(amino)thiophenol and 2-(methylthio)aniline were purchased from Aldrich Chemical Company.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(amino)thiophenol and 2-(methylthio)aniline were purchased from Aldrich Chemical Company.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Following the method described in Example 5 but substituting the product of the reaction of 2-(benzylthio)aniline and cinnamoyl chloride for the 2-(benzylthio)phenylacetanilide and using 1,5-dibromopentane in place of 1,4-dibromobutane, the title compound is obtained. This material was isolated as a pale yellow oil.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 2-(amino)thiophenol and 2-(methylthio)aniline were purchased from Aldrich Chemical Company.