1-Bromo-4-[(2,2-dimethoxyethyl)sulfanyl]benzene → 5-Bromo-1-benzothiophene

HRID 270011Notes

Reaction equation

HRID 270011 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH:10](OC)OC)=[CH:4][CH:3]=1>ClC1C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[S:8][CH:9]=[CH:10][C:4]=2[CH:3]=1

Participants

3

Procedure

A mixture of polyphosphoric acid (10 g) in chlorobenzene (260 mL) was heated to reflux and added, under nitrogen, dropwise in one hour 1-bromo-4-(2,2-dimethoxy-ethylsulfanyl)-benzene (compound PRE12; 9.71 g, 35 mmol). The reaction mixture was then heated for 4 h until reaction is complete, cooled, quenched with water (150 mL) and extracted into methylene chloride. Combined organic layer was dried over Na2SO4 and concentrated to give a crude residue that was purified by flash chromatography (silica, eluting solvent: petroleum ether) to give 3.8 g of 5-bromo-benzo[b]thiophene (white solid) (Yield=51%).

Workup

  1. temperaturewas heated
  2. temperatureto reflux
  3. temperatureThe reaction mixture was then heated for 4 h until reaction
  4. temperaturecooled
  5. customquenched with water (150 mL)
  6. extractionextracted into methylene chloride
  7. dry with materialCombined organic layer was dried over Na2SO4
  8. concentrationconcentrated
  9. customto give a crude residue that
  10. customwas purified by flash chromatography (silica, eluting solvent: petroleum ether)

Sources & evidence

ORD record
ord-f9571fdaf4c64417a23cc8e34b34d902
Source dataset
uspto-grants-2008_11
Patent number
US07449481B2

Reaction notes

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