1-Chloro-4-[(2,2-dimethoxyethyl)sulfanyl]benzene → 5-Chlorobenzo(b)thiophene

HRID 1013151Notes

Reaction equation

HRID 1013151 reaction equation
[Cl: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>[Cl: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 (11.2 g) in chlorobenzene (290 mL) was heated to reflux and added, under nitrogen, dropwise in about one hour 1-chloro-4-(2,2-dimethoxy-ethylsulfanyl)-benzene (compound PRE9; 9.12 g, 39.2 mmol). The reaction mixture was then heated for one night until reaction is complete, cooled, quenched with water (150 mL) and extracted into methylene chloride (200 mL). 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 2.1 g of 5-chloro-benzo[b]thiophene (limpid oil) (Yield=32%).

Workup

  1. temperaturewas heated
  2. temperatureto reflux
  3. temperatureThe reaction mixture was then heated for one night until reaction
  4. temperaturecooled
  5. customquenched with water (150 mL)
  6. extractionextracted into methylene chloride (200 mL)
  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-3a4f303aaea94474b526af65223efc17
Source dataset
uspto-grants-2011_07
Patent number
US07981907B2

Reaction notes

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