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Phosphorus oxychloride → 2-Chloro-4-(3-trifluoromethyl-phenyl)-thiazole

HRID 1667671
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HRID 1667671 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]([C:9]2[NH:10][C:11](=O)[S:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1.P(Cl)(Cl)([Cl:19])=O>>[Cl:19][C:11]1[S:12][CH:13]=[C:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([C:2]([F:16])([F:15])[F:1])[CH:4]=2)[N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 432867304-[3-(Trifluoromethyl)phenyl]-2,3-dihydro-1,3-thiazol-2-one

생성물 1

HCID 629425372-Chloro-4-(3-trifluoromethyl-phenyl)-thiazole수율 64.8%

실험 절차

A mixture of 24.55 g (100.1 mmole) of 4-(3-trifluoromethyl-phenyl)-3H-thiazol-2-one and 75 mL (0.811 mole) of phosphorus oxychloride was heated at reflux for 3 hours. The cooled mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate and poured onto ice. The mixture was made basic by the addition of saturated sodium carbonate solution. The ethyl acetate layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 10:90-20:80) to give 17.09 g of 2-chloro-4-(3-trifluoromethyl-phenyl)-thiazole as a light brown solid.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 3 hours
  3. concentrationThe cooled mixture was concentrated under reduced pressure
  4. additionThe residue was diluted with ethyl acetate
  5. additionpoured onto ice
  6. additionThe mixture was made basic by the addition of saturated sodium carbonate solution
  7. dry with materialThe ethyl acetate layer was dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by silica gel chromatography
  11. washeluting with ethyl acetate-hexanes (gradient 10:90-20:80)

출처 및 근거

ORD 기록
ord-407d0c95560848a88b584feee77a1a98
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044213B2

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