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Sodium Iodide → 1-Benzyloxy-2-iodoethane

HRID 428963
ノート
印刷プレビュー

反応式

HRID 428963 の反応式
BrC1C=CC(S(O[CH2:12][CH2:13][O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)(=O)=O)=CC=1.[I-:22].[Na+]>CC(C)=O>[I:22][CH2:12][CH2:13][O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=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 20702450(Benzyloxy)ethyl 4-bromobenzenesulfonate

生成物 1

HCID 103553141-Benzyloxy-2-iodoethane収率 88.1%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a solution of (benzyloxy)ethyl 4-bromobenzenesulfonate (Preparation 89, 6.92 g, 19.5 mmol) in acetone (60 ml) was added sodium iodide (5.84 g, 39.0 mmol) and the reaction mixture was left to stir at room temperature for 16 h. The resulting precipitate was filtered and the filtrate was concentrated in vacuo. The crude residue was dissolved in dichloromethane and washed with aqueous sodium thiosulphate solution and then with water (2×60 ml). The organic layer was dried (Na2SO4) and concentrated in vacuo to give the title compound as a pale brown oil (4.5 g, 88%).

後処理

  1. waitthe reaction mixture was left
  2. filtrationThe resulting precipitate was filtered
  3. concentrationthe filtrate was concentrated in vacuo
  4. dissolutionThe crude residue was dissolved in dichloromethane
  5. washwashed with aqueous sodium thiosulphate solution
  6. dry with materialThe organic layer was dried (Na2SO4)
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-4e03dfb26ace47de9bf4efe08ebfb3c6
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313312B1

反応ノート

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