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Chlorosulfonic acid → 2-Ethoxy-5-methylbenzene-1-sulfonyl chloride

HRID 342381
ノート
印刷プレビュー

反応式

HRID 342381 の反応式
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[CH:6][CH:5]=1)[CH3:2].[Cl:11][S:12](O)(=[O:14])=[O:13]>ClCCl>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[CH:6][C:5]=1[S:12]([Cl:11])(=[O:14])=[O:13])[CH3:2]
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 24638Chlorosulfonic acidHCID 73955Benzene, 1-ethoxy-4-methyl-

生成物 1

HCID 183661972-Ethoxy-5-methylbenzene-1-sulfonyl chloride

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 6.8 g (50 mmol) of 4-ethoxy-toluene in 20 mL of dichloromethane was added to a solution of 10 mL (150 mmol) of chlorosulfonic acid in 10 mL of dichloromethane at 0° C. with cooling and stirring. The mixture was stirred 1 hour at 0° C. and was then warmed to ambient temperature and stirred another hour. The resulting tan solution was poured into 200 mL of ice water and the mixture was extracted with dichloromethane. The extract was dried over magnesium sulfate and concentrated by evaporation under reduced pressure. The residual 7.9 g (68 percent of theory) of light tan solid melting at 59°-61° C. was the title compound.

後処理

  1. temperaturewith cooling
  2. stirringThe mixture was stirred 1 hour at 0° C.
  3. stirringstirred another hour
  4. extractionthe mixture was extracted with dichloromethane
  5. dry with materialThe extract was dried over magnesium sulfate
  6. concentrationconcentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-7bcc6fdbffbd439b98e75d1c1458f51b
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05858924

反応ノート

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