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

HRID 616727

반응식

HRID 616727 반응식
[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]

참가 물질

4

반응물 3

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

생성물 1

HCID 27360942,5-Dichlorothiophene-3-sulfonyl chloride

반응 조건

온도
50 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-202c4b75f6e242a8ae686f3407338284
출처 데이터셋
uspto-grants-1978_02
특허 번호
US04075347

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