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Isopropyl iodide → HCID 43657408, 화합물

HRID 870521
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HRID 870521 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[OH:10])[C:5]#[N:6].[CH:11](I)([CH3:13])[CH3:12].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[O:10][CH:11]([CH3:13])[CH3:12])[C:5]#[N:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 27829443-Fluoro-4-hydroxybenzonitrile

생성물 1

HCID 43657408HCID 43657408, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

5.0 g 3-Fluoro-4-hydroxy-benzonitrile, 7.3 mL isopropyl iodide and 6.05 g potassium carbonate were placed in 54 mL acetone and heated to reflux where the reaction was maintained for 24 h. After this time, the mixture was cooled to ambient temperature and concentrated under reduced pressure. The material that remained was partitioned between ethyl acetate and water and the aqueous phase was removed and extracted with additional ethyl acetate. The combined organics were dried, filtered and the solvent was removed from the filtrate under reduced pressure to give the title compound that was used without further purification.

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후처리

  1. temperatureheated
  2. temperatureto reflux where the reaction
  3. temperaturewas maintained for 24 h
  4. concentrationconcentrated under reduced pressure
  5. customThe material that remained was partitioned between ethyl acetate and water
  6. customthe aqueous phase was removed
  7. extractionextracted with additional ethyl acetate
  8. customThe combined organics were dried
  9. filtrationfiltered
  10. customthe solvent was removed from the filtrate under reduced pressure

출처 및 근거

ORD 기록
ord-632669bc85c34945bbe87d146d9b5638
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969568B2

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