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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Benzofuransulfonamide(9CI)

HRID 260646
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HRID 260646 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([S:10]([NH2:13])(=[O:12])=[O:11])=[CH:9][C:4]=2[CH2:3][CH2:2]1.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>O1CCOCC1>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([S:10]([NH2:13])(=[O:11])=[O:12])=[CH:9][C:4]=2[CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 108996192,3-Dihydro-1-benzofuran-5-sulfonamide

생성물 1

HCID 158411515-Benzofuransulfonamide(9CI)수율 18%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A suspension of 2,3-dihydrobenzofuran-5-sulfonamide (19.9 g, 100 mmol) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) (56.7 g, 250 mmol) in dioxane (500 ml) was heated at reflux under nitrogen for 111 hours. The reaction mixture was reduced in volume by evaporation under vacuum and purified by silica gel flash chromatography (EtOAc/hexanes) to provide benzofuran-5-sulfonamide (3.5 g, 18% ) . This was combined with another lot of benzofuran-5-sulfonamide (1.0 g), slurried in ether, collected and vacuum dried at 45° C. overnight to give 4.5 g of benzofuran-5-sulfonamide.

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후처리

  1. temperaturewas heated
  2. temperatureat reflux under nitrogen for 111 hours
  3. customThe reaction mixture was reduced in volume by evaporation under vacuum
  4. custompurified by silica gel flash chromatography (EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-f81ea3fe3b264064b1a502ed3d366e7a
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05529999

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