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Formamide → 2-Fluoro-4-(thiazol-4-yl)phenol

HRID 2086745
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HRID 2086745 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]([OH:28])=[C:24]([F:29])[CH:23]=1)=O.[CH:30]([NH2:32])=[S:31].[OH-].[Na+]>O1CCOCC1>[F:29][C:24]1[CH:23]=[C:22]([C:20]2[N:32]=[CH:30][S:31][CH:19]=2)[CH:27]=[CH:26][C:25]=1[OH:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 713FormamideHCID 14798Sodium HydroxideHCID 14817Phosphorus sulfide (P2S5)HCID 3005587MethanethioamideHCID 179235302-Bromo-1-(3-fluoro-4-hydroxyphenyl)ethan-1-one

생성물 1

HCID 223169222-Fluoro-4-(thiazol-4-yl)phenol수율 83%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

To a stirred solution of phosphorus pentasulfide (8.6 g, 19.3 mmol) in dioxane (53 ml) was added formamide (5.2 g, 115.5 mmol), and the mixture was heated at reflux temperature for 2 hours. The mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(3-fluoro-4-hydroxyphenyl)-1-ethanone (3.02 g, 12.98 mmol) in dioxane (50 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The mixture was cooled down to room temperature, and made basic by addition of 0.5M NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:3) to give title compound (2.11 g, 83% 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 mixture was cooled down to room temperature
  7. extractionThe whole was extracted with ethyl acetate
  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 ethyl acetate-hexane (1:3)

출처 및 근거

ORD 기록
ord-e47de7ac2fc742619e5fe700be352675
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06727238B2

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