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Chlorosulfonic acid → 4-(2-Methylpropoxy)benzene-1-sulfonyl chloride

HRID 1406552
ノート
印刷プレビュー

反応式

HRID 1406552 の反応式
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH:2]([CH3:4])[CH3:3].[Cl:12][S:13](O)(=[O:15])=[O:14]>ClCCl>[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([S:13]([Cl:12])(=[O:15])=[O:14])=[CH:8][CH:7]=1)[CH:2]([CH3:4])[CH3:3]
参加物反応条件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 24638Chlorosulfonic acid2 回HCID 254373(2-Methylpropoxy)benzene

生成物 1

HCID 125711294-(2-Methylpropoxy)benzene-1-sulfonyl chloride収率 28%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-45 °C

実験手順

To a stirring solution of isobutoxybenzene (0.60 g, 4.0 mmol) in dichloromethane (5 mL) at −45° C. was added chlorosulfonic acid (0.6 mL, 9.1 mmol) dropwise, and the reaction mixture was stirred at −45° C. for 1 h. The reaction mixture was then warmed to 0° C. and additional chlorosulfonic acid (0.6 mL, 9.1 mmol) was added dropwise. The reaction mixture was then stirred at 0° C. for 1 h and poured into ice. The aqueous layer was extracted with ethyl acetate and the organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2, 5-10% ethyl acetate in hexanes) to give 4-isobutoxybenzene-1-sulfonyl chloride (0.32 g, 1.1 mmol, 28%).

後処理

  1. temperatureThe reaction mixture was then warmed to 0° C.
  2. stirringThe reaction mixture was then stirred at 0° C. for 1 h
  3. additionpoured into ice
  4. extractionThe aqueous layer was extracted with ethyl acetate
  5. dry with materialthe organic layer was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was purified by flash chromatography (SiO2, 5-10% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-4140584514834af1a21b7d886144ff60
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08916601B2

反応ノート

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