Thiophene → HCID 12060894, compound

HRID 486828Notes

Reaction equation

HRID 486828 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)N.C(ON=O)CC(C)C.[S:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1>CCOCC>[Br:1][C:2]1[CH:3]=[C:4]([C:18]2[S:17][CH:21]=[CH:20][CH:19]=2)[CH:6]=[CH:7][CH:8]=1

Participants

5

Procedure

To a stirred solution of m-bromoaniline (34.4 g; 0.2M) in thiophene (200 mL) was added isoamylnitrite (46.86 g; 0.4M) dropwise over a period of 30 mins. at 0° C. The resulting mixture was cautiously warmed to R.T. and heated to reflux for 16 hours. The reaction mixture was cooled, diluted with 400 mL of ether, washed with 3×100 mL of satd. sodium chloride solution, and dried over anhydrous magnesium sulfate. Solvent and excess thiophene were removed. A solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed. Solvent was removed, and the residue was distilled to give 34% of 2-(3'-bromophenyl) thiophene as a yellow liquid boiling at 130°-2°/~0.2 mm. This liquid solidified on standing in the refrigerator.

Workup

  1. customat 0° C
  2. temperatureheated
  3. temperatureto reflux for 16 hours
  4. temperatureThe reaction mixture was cooled
  5. washwashed with 3×100 mL of satd
  6. dry with materialsodium chloride solution, and dried over anhydrous magnesium sulfate
  7. customSolvent and excess thiophene were removed
  8. filtrationA solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed
  9. customSolvent was removed
  10. distillationthe residue was distilled

Sources & evidence

ORD record
ord-2ff315e628354f3a8175500c13086f3a
Source dataset
uspto-grants-1994_03
Patent number
US05292879

Reaction notes

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