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Isopropyl iodide → HCID 43657408、化合物

HRID 715691
ノート
印刷プレビュー

反応式

HRID 715691 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 43657408HCID 43657408、化合物

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-83dcf9b847f84eec93bc5f8fd2589558
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187478B2

反応ノート

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