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4-But-2-ynyloxy-benzenesulfonyl chloride → 4-But-2-ynyloxybenzenesulfonyl fluoride

HRID 353562
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인쇄 미리보기

반응식

HRID 353562 반응식
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([S:12](Cl)(=[O:14])=[O:13])=[CH:8][CH:7]=1)[C:2]#[C:3][CH3:4].[F-:16].[K+].[F-].[F-].[Ca+2]>>[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([S:12]([F:16])(=[O:14])=[O:13])=[CH:8][CH:7]=1)[C:2]#[C:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 111959284-But-2-ynyloxy-benzenesulfonyl chlorideHCID 23699612Calcium;potassium;trifluoride

생성물 1

HCID 111955204-But-2-ynyloxybenzenesulfonyl fluoride수율 80.3%

실험 절차

To a solution of 4-but-2-ynyloxybenzenesulfonyl chloride (prepared from Example 30, step 4) (2.0 g, 8.18 mmol) in acetonitrle (10 ml) was added KF-CaF2 (2.85 g, 16.3 mmol) and the resulting mixture was stirred for 4 hours at room temperature. The reaction mixture was filtered and the filterate was concentrated. The crude product was dissolved in EtOAc and washed with water. The organic layer was dried over anhydrous Na2SO4 and the solvent was removed to obtain 1.5 g (80%) of the product as solid.

후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filterate was concentrated
  3. dissolutionThe crude product was dissolved in EtOAc
  4. washwashed with water
  5. dry with materialThe organic layer was dried over anhydrous Na2SO4
  6. customthe solvent was removed

출처 및 근거

ORD 기록
ord-aa4edae5bb024e578df609a95718aa8d
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06753337B2

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