2,5-Dichlorothiophene → 2,5-Dichlorothiophene-3-sulfonyl chloride

HRID 616727

反応式

HRID 616727 の反応式
[Cl:1][C:2]1[S:3][C:4]([Cl:7])=[CH:5][CH:6]=1.C(=O)=O.CC(C)=O.[Cl:15][S:16](O)(=[O:18])=[O:17]>>[Cl:1][C:2]1[S:3][C:4]([Cl:7])=[CH:5][C:6]=1[S:16]([Cl:15])(=[O:18])=[O:17]

参加物

4

反応物 3

HCID 185012,5-DichlorothiopheneHCID 24638Chlorosulfonic acidHCID 18522661Acetone cardice

生成物 1

HCID 27360942,5-Dichlorothiophene-3-sulfonyl chloride

反応条件

温度
50 °C

実験手順

A 96.8-g (0.632 mol) sample of 2,5-dichlorothiophene was added dropwise to a cooled (dry ice/acetone bath, about -10° to -15° C.) and stirred solution of 163 g (1.39 mol) of chlorosulfonic acid. After the addition was completed, the reaction mixture was stirred at 50° C for 2 hours, cooled, and then poured into 200 g of ice. The aqueous reaction mixture was extracted with methylene chloride. The methylene chloride extract was washed with saturated aqueous sodium bicarbonate solution, washed with water, dried over magnesium sulfate, and evaporated to give 87 g of 2,5-dichloro-3-thienylsulfonyl chloride.

後処理

  1. additionAfter the addition
  2. temperaturecooled
  3. extractionThe aqueous reaction mixture was extracted with methylene chloride
  4. extractionThe methylene chloride extract
  5. washwas washed with saturated aqueous sodium bicarbonate solution
  6. washwashed with water
  7. dry with materialdried over magnesium sulfate
  8. customevaporated

出典と根拠

ORDレコード
ord-202c4b75f6e242a8ae686f3407338284
出典データセット
uspto-grants-1978_02
特許番号
US04075347

関連ノート

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