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Bromine → 4-Bromo-1-(methylthio)-2-(trifluoromethyl)-benzene

HRID 748899
Notes
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Reaction equation

HRID 748899 reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([F:12])([F:11])[F:10].[Br:13]Br.[Cl-].[Al+3].[Cl-].[Cl-].S([O-])([O-])(=O)=S.[Na+].[Na+]>[Fe].C(OCC)(=O)C.O.ClCCl>[Br:13][C:6]1[CH:7]=[CH:8][C:3]([S:2][CH3:1])=[C:4]([C:9]([F:10])([F:11])[F:12])[CH:5]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

9

Reactant 4

HCID 24408BromineHCID 24477Sodium ThiosulfateHCID 27607832-TrifluoromethylthioanisoleHCID 6451240Aluminum(III) Chloride

Product 1

HCID 223153184-Bromo-1-(methylthio)-2-(trifluoromethyl)-benzeneYield 83%

Reagents, catalysts & solvents 4

HCID 23925
Iron
Catalyst
HCID 962WaterSolvent
HCID 6344DichloromethaneSolvent
HCID 8857Ethyl AcetateSolvent

Procedure

Combine 1-methylsulfanyl-2-trifluoromethyl-benzene (3.5 g, 18 mmol), iron (100 mg, 1.79 mmol), bromine (0.95 mL, 18 mmol), aluminum chloride (242 mg, 1.8 mmol) and dichloromethane (50 mL) and stir for 2 hours. Add water (10 mL), aqueous saturated sodium thiosulfate (100 mL) and ethyl acetate (100 mL). Separate the organic layer and wash with brine, dry with MgSO4, filter and concentrate in vacuo. Chromatograph the residue on a SiO2 column eluting with hexane to give 3.6 g of 4-bromo-1-methylsulfanyl-2-trifluoromethyl-benzene (83%).

Workup

  1. customSeparate the organic layer
  2. washwash with brine
  3. dry with materialdry with MgSO4
  4. filtrationfilter
  5. concentrationconcentrate in vacuo
  6. washChromatograph the residue on a SiO2 column eluting with hexane

Sources & evidence

ORD record
ord-364a549288a3412aa83d2f8b162fff16
Source dataset
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07399867B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes