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4-Chlorotoluene → Tris(4-methylphenyl)sulfanium Chloride

HRID 424327
Notes
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Reaction equation

HRID 424327 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)=O)=[CH:4][CH:3]=1.[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=1>O>[Cl-:17].[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S+:8]([C:18]2[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=2)[C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 78104-ChlorotolueneHCID 15680p-Tolyl sulfoxide

Product 1

HCID 5351245Tris(4-methylphenyl)sulfanium Chloride

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The target compound was obtained by following the procedure of Synthesis Example 1-1 aside from using bis(4-methylphenyl) sulfoxide instead of the diphenyl sulfoxide and 4-chlorotoluene instead of the chlorobenzene in Synthesis Example 1-1, and increasing the amount of water for extraction.

Workup

  1. custom
The target compound was obtained
  • customthe procedure of Synthesis Example 1-1 aside
  • customin Synthesis Example 1-1
  • extractionfor extraction
  • Sources & evidence

    ORD record
    ord-cc04e438ef3d497684ccfa4473f16555
    Source dataset
    uspto-grants-2012_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08105748B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes