HCID 67047335, compound → 7-Bromobenzo[b]thiophene

HRID 1783970Notes

Reaction equation

HRID 1783970 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][CH:9]=[CH:10]OCC>ClC1C=CC=CC=1>[Br:1][C:2]1[C:3]2[S:8][CH:9]=[CH:10][C:4]=2[CH:5]=[CH:6][CH:7]=1

Participants

3

Conditions

Temperature
70 °C

Procedure

1-Bromo-2-(2-ethoxyvinylsulfanyl)benzene is dissolved in chlorobenzene (50 mL) and the solution is heated to 70° C. PPA (10.5 mL) is then added carefully and the biphasic mixture is heated at 150° C. overnight. The resulting dark syrup is allowed to cool down and the supernatant solvent removed by pipette. Chlorobenzene (15 mL) is added to the residue and heated to 150° C. for 30 min. The solvent is removed again and the residue washed with small amounts of dichloromethane until the washings are clear. The organic fractions are combined and filtered through celite to afford a clear yellow solution. Concentration under vacuum followed by LC using cyclohexane as the eluent provided the title compound as a viscous colourless oil (1.21 g, 35%).

Workup

  1. additionPPA (10.5 mL) is then added carefully
  2. temperaturethe biphasic mixture is heated at 150° C. overnight
  3. temperatureto cool down
  4. customthe supernatant solvent removed by pipette
  5. additionChlorobenzene (15 mL) is added to the residue
  6. temperatureheated to 150° C. for 30 min
  7. customThe solvent is removed again
  8. washthe residue washed with small amounts of dichloromethane until the washings
  9. filtrationfiltered through celite
  10. customto afford a clear yellow solution
  11. concentrationConcentration under vacuum

Sources & evidence

ORD record
ord-25bb78cf37ed41c68f9f83ba102f470d
Source dataset
uspto-grants-2009_03
Patent number
US07501411B2

Reaction notes

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