Quinoline → 4-Chloro-1-benzothiophene

HRID 2183585Notes

Reaction equation

HRID 2183585 reaction equation
[Cl:1][C:2]1[C:10]2[CH:9]=[C:8](C(O)=O)[S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.N1C2C(=CC=CC=2)C=CC=1>[Cu].Cl>[Cl:1][C:2]1[C:10]2[CH:9]=[CH:8][S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1

Participants

5

Procedure

A mixture of 4-chlorobenzo[b]thiophene-2-carboxylic acid (2 g prepared in a manner similar to that described in J. Chem. Res. (S), 1978, 10), copper powder (0.82 g) and quinoline (20 ml) was stirred under nitrogen at 180° C. for 2 hours then cooled to ambient temperature and acidified by the addition of 2M hydrochloric acid (50 ml). The product was extracted into ether (50 ml), the extract was dried (MgSO4) and the solvent was removed in vacuo. The residue was purified by flash chromatography over silica using a 5:1 mixture of petroleum ether (b.p. 60-80° C.) and ethyl acetate as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 4-chlorobenzo[b]thiophene (1.49 g) as a pale yellow oil which was used without further purification.

Workup

  1. customprepared in a manner similar to
  2. extractionThe product was extracted into ether (50 ml)
  3. dry with materialthe extract was dried (MgSO4)
  4. customthe solvent was removed in vacuo
  5. customThe residue was purified by flash chromatography over silica using
  6. additiona 5:1 mixture of petroleum ether (b.p. 60-80° C.) and ethyl acetate as eluant
  7. customthe solvents removed in vacuo

Sources & evidence

ORD record
ord-498f0715e529484880091965cb579656
Source dataset
uspto-grants-2005_05
Patent number
US06900216B2

Reaction notes

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