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2,6-Dichlorobenzoic acid → 2,6-Dichloro-3-(chlorosulfonyl)benzoic acid

HRID 1368828
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HRID 1368828 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([Cl:11])[C:3]=1[C:4]([OH:6])=[O:5].[Cl:12][S:13](O)(=[O:15])=[O:14]>>[Cl:12][S:13]([C:8]1[C:7]([Cl:11])=[C:3]([C:2]([Cl:1])=[CH:10][CH:9]=1)[C:4]([OH:6])=[O:5])(=[O:15])=[O:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 57582,6-Dichlorobenzoic acidHCID 24638Chlorosulfonic acid

생성물 1

HCID 35382162,6-Dichloro-3-(chlorosulfonyl)benzoic acid수율 61%

반응 조건

온도
10 °C

실험 절차

Part A: Under an atmosphere of nitrogen gas, a reaction vessel was charged with 2,6-dichlorobenzoic acid (10 g, 53.55 mmol) (Formula F) and chlorosulfonic acid (3 ml, 472 mmol). The reaction mixture was refluxed for 1 hour and cooled to 10° C. The contents of the reaction vessel were poured slowly into 3 L of ice water. The white solid which precipitated was collected by filtration and dried in vacuo (10 mm) at 35° C. for 48 hours to give 3-(chlorosulfonyl)-2,6-dichlorobenzoic acid (Formula G) (9.2 g, 61% yield).

후처리

  1. temperatureThe reaction mixture was refluxed for 1 hour
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  • customThe white solid which precipitated
  • filtrationwas collected by filtration
  • customdried in vacuo (10 mm) at 35° C. for 48 hours
  • 출처 및 근거

    ORD 기록
    ord-520feb4ddec047b0bc144d3d441bc02c
    출처 데이터셋
    uspto-grants-2003_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06576614B1

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