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Thionyl Chloride → [(2-Chloroethyl)selanyl]benzene

HRID 977422
ノート
印刷プレビュー

反応式

HRID 977422 の反応式
[C:1]1([Se:7][CH2:8][CH2:9]O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:13])=O>C(Cl)Cl>[Cl:13][CH2:9][CH2:8][Se:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=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 24386Thionyl ChlorideHCID 11030856Ethanol, 2-(phenylseleno)-2 回

生成物 1

HCID 14699146[(2-Chloroethyl)selanyl]benzene

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

One gram of the resulting 2-hydroxyethyl phenyl selenide was dissolved in 15 ml of CH2Cl2. One ml of thionyl chloride was dissolved in 5 ml of CH2Cl2 and was added to the solution of the 2-hydroxyethyl phenyl selenide. The reaction mixture was refluxed for 1 h. The solvent was evaporated off and the remaining product transferred to a separatory funnel using CHCl3. Twenty ml of water was added to the separatory funnel and was made weakly basic with 5% aqueous NaHCO3. The CHCl3 layer was removed from the separatory funnel, dried with sodium sulfate and removed from the product by rotary evaporation and then in vacuo.

後処理

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. customThe solvent was evaporated off
  3. customthe remaining product transferred to a separatory funnel
  4. additionTwenty ml of water was added to the separatory funnel
  5. customThe CHCl3 layer was removed from the separatory funnel
  6. dry with materialdried with sodium sulfate
  7. customremoved from the product by rotary evaporation

出典と根拠

ORDレコード
ord-d7b4543fe6064b96a7353b5e431836e3
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05614562

反応ノート

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