Formamide → 4-(4-Bromophenyl)thiazole

HRID 497221노트

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HRID 497221 반응식
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

참가 물질

7

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-a1bae95be9284c5b83dee0f2d7b8a7d2
출처 데이터셋
uspto-grants-2005_09
특허 번호
US06949536B2

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