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3-Chloro-4-hydroxybenzoic acid → 3-Chloro-5-(chlorosulfonyl)-4-hydroxybenzoic acid

HRID 1889689
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인쇄 미리보기

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HRID 1889689 반응식
[Cl:1][S:2]([OH:5])(=O)=[O:3].[Cl:6][C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][C:15]=1[OH:16])[C:10]([OH:12])=[O:11]>>[Cl:6][C:7]1[CH:8]=[C:9]([CH:13]=[C:14]([S:2]([Cl:1])(=[O:5])=[O:3])[C:15]=1[OH:16])[C:10]([OH:12])=[O:11]
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참가 물질

3

반응물 2

HCID 198603-Chloro-4-hydroxybenzoic acidHCID 24638Chlorosulfonic acid

생성물 1

HCID 545935123-Chloro-5-(chlorosulfonyl)-4-hydroxybenzoic acid수율 74.2%

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온도
65 °C

실험 절차

To a flask charged with chlorosulfonic acid (13.9 mL, 209.0 mmol) was added 3-chloro-4-hydroxybenzoic acid (6.0 g, 34.8 mmol) portionwise over ten minutes. The mixture was then heated for 2 h at 65° C. under a nitrogen atmosphere. After cooling the mixture to room temperature, the reaction mixture was carefully poured over crushed ice with vigorous stirring, and extracted with Et2O until no further product remained in the aqueous layer. The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo to afford 3-chloro-5-(chlorosulfonyl)-4-hydroxy-benzoic acid as a white solid (7.0 g, 74%) which was used without further purification.

후처리

  1. temperatureAfter cooling the mixture to room temperature
  2. additionthe reaction mixture was carefully poured
  3. customover crushed ice with vigorous stirring
  4. extractionextracted with Et2O until no further product
  5. dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-eee0062f1bd8493f915096a8259e9162
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501992B2

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