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2,6-Dichlorotoluene → 2,4-Dichloro-3-methylbenzene-1-sulfonyl chloride

HRID 1990717
ノート
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反応式

HRID 1990717 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[CH3:9].[Cl:10][S:11](O)(=[O:13])=[O:12]>>[Cl:1][C:2]1[C:3]([CH3:9])=[C:4]([Cl:8])[CH:5]=[CH:6][C:7]=1[S:11]([Cl:10])(=[O:13])=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 83682,6-DichlorotolueneHCID 24638Chlorosulfonic acid

生成物 1

HCID 157253742,4-Dichloro-3-methylbenzene-1-sulfonyl chloride収率 85%

実験手順

10 ml of chlorosulfonic acid were dropwise added with 4.8 ml of 2,6-dichlorotoluene in two hours, under magnetic stirring at room temperature. After completion of the addition, the mixture was heated at 40° C. for two hours, thereby obtaining a purple solution, which was cooled and carefully poured into ice-water (0.5 l), stirring vigorously. The separated white solid was filtered, triturated, washed with water, dried over KOH and purified by washing with n-hexane, adding 200 ml of solvent under strong stirring. The mixture was filtered, the solid was discarded and the solvent was evaporated to dryness to obtain 2,4-dichloro-3-methyl-benzenesulfonyl chloride as a crystalline white solid. Yield: 85%.

後処理

  1. additionAfter completion of the addition
  2. temperature
the mixture was heated at 40° C. for two hours
  • customobtaining a purple solution, which
  • temperaturewas cooled
  • stirringstirring vigorously
  • filtrationThe separated white solid was filtered
  • customtriturated
  • washwashed with water
  • dry with materialdried over KOH
  • custompurified
  • washby washing with n-hexane
  • additionadding 200 ml of solvent under strong stirring
  • filtrationThe mixture was filtered
  • customthe solvent was evaporated to dryness
  • 出典と根拠

    ORDレコード
    ord-914016fb3d204dc2b3f71db600191261
    出典データセット
    uspto-grants-2010_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07645759B2

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