Methyl iodide → 2-[(Methylsulfanyl)methyl]-1,1'-biphenyl

HRID 270006Notes

Reaction equation

HRID 270006 reaction equation
[C:1]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][SH:8].[CH3:15]I>CO.C[O-].[Na+]>[CH3:15][S:8][CH2:7][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

A mixture of biphenyl-2-yl-methanethiol (4 g, 20 mmol) in methanol (27 mL) and sodium methoxide in methanol (0.5 M, 40 mL) was heated at 60° C. for 0.5 h, cooled, treated with methyl iodide (3.7 mL, 60 mmol) and re-heated at 60° C. for 0.5 h. After cooling to room temperature, the reaction mixture was quenched with ice-water, acidified (pH˜2) and extracted with ethyl acetate (3×50 mL). Combined organic layer was washed with water (1×50 mL) and brine (1×50 mL), dried (MgSO4), and concentrated to give a crude product that was passed through a bed of silica (solvent: ethyl acetate) to give 3.3 g of 2-methylsulfanylmethyl-biphenyl (yellow oil) that was directly used in the next step.

Workup

  1. temperaturecooled
  2. temperaturere-heated at 60° C. for 0.5 h
  3. temperatureAfter cooling to room temperature
  4. customthe reaction mixture was quenched with ice-water
  5. extractionextracted with ethyl acetate (3×50 mL)
  6. washCombined organic layer was washed with water (1×50 mL) and brine (1×50 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customto give a crude product that

Sources & evidence

ORD record
ord-0a67617748a844a382de08be843f5cfb
Source dataset
uspto-grants-2008_11
Patent number
US07449481B2

Reaction notes

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