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Thionyl Chloride → 1-(Chloromethyl)-4-(4-phenylbutoxy)benzene

HRID 1739403
ノート
印刷プレビュー

反応式

HRID 1739403 の反応式
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH2:16]O)=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:22])=O>C(Cl)(Cl)Cl>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH2:16][Cl:22])=[CH:14][CH:13]=2)[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 540346054-(4-Phenylbutoxy)benzyl alcohol

生成物 1

HCID 151155321-(Chloromethyl)-4-(4-phenylbutoxy)benzene収率 102.9%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

2.9 g of 4-(4-phenylbutyloxy)benzyl alcohol were dissolved in 30 ml of chloroform, and 1.6 g of thionyl chloride were further fed dropwise to the resultant solution. The solution was then stirred for 1 hour at room temperature. After completed the reaction, the solution reacted was poured into ice-water and extracted with chloroform. The organic layer resulted was dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure, thereby affording 3.2 g of 4-(4-phenylbutyloxy)benzyl chloride.

後処理

  1. customthe reaction
  2. customthe solution reacted
  3. extractionextracted with chloroform
  4. customThe organic layer resulted
  5. dry with materialwas dried with anhydrous magnesium sulfate
  6. customthe solvent used was removed by distillation under reduced pressure

出典と根拠

ORDレコード
ord-e90f10463560454484813b7b1dbc222d
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05965743

反応ノート

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