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Sodium Iodide → HCID 69799308、化合物

HRID 2179938
ノート
印刷プレビュー

反応式

HRID 2179938 の反応式
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([O:10][C@@H:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:12][CH2:13]Cl)[CH:3]=1.[I-:21].[Na+]>CC(C)=O>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([O:10][C@@H:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:12][CH2:13][I:21])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5238Sodium IodideHCID 20779195HCID 20779195、化合物

生成物 1

HCID 69799308HCID 69799308、化合物収率 84%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

4-Chloro-2-{[(1R)-3-chloro-1-phenylpropyl]oxy}benzonitrile (220mg, 0.718 mmol) was dissolved in acetone (20 ml) which had previously been saturated with sodium iodide and the solution was heated under reflux for 18 h. The reaction mixture was cooled, filtered, evaporated and the residue partitioned between water and ethyl acetate. The organic layer was separated, washed twice with water and dried (magnesium sulphate). The solvent was evaporated to leave 0.24 g (84%) of the product as a yellow oil. This was used without purification for the next step.

後処理

  1. temperaturethe solution was heated
  2. temperatureunder reflux for 18 h
  3. temperatureThe reaction mixture was cooled
  4. filtrationfiltered
  5. customevaporated
  6. customthe residue partitioned between water and ethyl acetate
  7. customThe organic layer was separated
  8. washwashed twice with water
  9. dry with materialdried (magnesium sulphate)
  10. customThe solvent was evaporated

出典と根拠

ORDレコード
ord-ec757257be6f47069bdcb43ee8ad3701
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06887871B2

反応ノート

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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