Formamide → 4-(4-Bromophenyl)thiazole

HRID 2086670Notes

Reaction equation

HRID 2086670 reaction equation
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=S.C(N)=O.Br[CH2:19][C:20]([C:22]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][CH:23]=1)=O.[CH:29]([NH2:31])=[S:30].[OH-].[Na+]>O1CCOCC1>[Br:28][C:25]1[CH:26]=[CH:27][C:22]([C:20]2[N:31]=[CH:29][S:30][CH:19]=2)=[CH:23][CH:24]=1

Participants

7

Procedure

To a stirred solution of phosphorus pentasulfide (24.5 g, 55 mmol) in dioxane (250 ml) was added formamide (28.4 g, 630 mmol), and the mixture was heated at reflux temperature for 2 hours. The reaction mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2,4′-dibromoacetophenone (15 g, 54 mmol) in dioxane (100 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 2N NaOH aqueous solution. The whole was extracted with diethyl ether. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with CH2Cl2 to give title compound (12.3 g, 95% yield).

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux temperature for 2 hours
  3. customthe solution was decanted away from solids
  4. temperaturethe mixture was heated
  5. temperatureat reflux temperature for 6 hours
  6. temperatureThe reaction mixture was cooled down to room temperature
  7. extractionThe whole was extracted with diethyl ether
  8. washThe organic layer was washed with brine
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. customThe residue was purified by flash chromatography
  12. washeluting with CH2Cl2

Sources & evidence

ORD record
ord-2fe3d745383c43d2be4e5bb8200e01eb
Source dataset
uspto-grants-2004_04
Patent number
US06727238B2

Reaction notes

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