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1-Bromo-3,5-difluorobenzene → 1-Bromo-3-fluoro-5-(methylsulfanyl)benzene

HRID 1887984
Notes
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Reaction equation

HRID 1887984 reaction equation
[Br:1][C:2]1[CH:7]=[C:6](F)[CH:5]=[C:4]([F:9])[CH:3]=1.[CH3:10][S-:11].[Na+]>CN(C)C=O>[Br:1][C:2]1[CH:7]=[C:6]([S:11][CH3:10])[CH:5]=[C:4]([F:9])[CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 1363131-Bromo-3,5-difluorobenzeneHCID 4378561Sodium methanethiolate

Product 1

HCID 534144401-Bromo-3-fluoro-5-(methylsulfanyl)benzene

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
150 °C

Procedure

To a solution of 1-bromo-3,5-difluorobenzene (5.0 g, 25.9 mmol) in dimethylformamide (40 ml) was added sodiumthiomethylate (1.81 g, 25.9 mmol), and the mixture was heated to 150° C. for 10 min. The reaction mixture was brought to ambient temperature, quenched with saturated aqueous ammonium chloride (100 ml) and extracted with ethylacetate (3×100 ml). The combined organic phases was dried and concentrated in vacuo to receive the pure title compound (3.84 g). MS m/z (rel. intensity, 70 eV) 222 (M+, 100), 220 (M+, 100), 189 (49), 187 (50), 126 (75).

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customwas brought to ambient temperature
  2. customquenched with saturated aqueous ammonium chloride (100 ml)
  3. extractionextracted with ethylacetate (3×100 ml)
  4. customThe combined organic phases was dried
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ef19c52ec3fb43ea8415c457ee1025ab
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08501777B2

Reaction notes

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