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4-Fluorobenzenesulfonyl chloride → 4-Fluorobenzenesulfonyl fluoride

HRID 60415
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HRID 60415 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[F-:12].[K+].C([O-])(O)=O.[Na+]>C(#N)C.C1OCCOCCOCCOCCOCCOC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([F:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 95884-Fluorobenzenesulfonyl chlorideHCID 516892Sodium BicarbonateHCID 522689Potassium Fluoride

생성물 1

HCID 30819424-Fluorobenzenesulfonyl fluoride수율 102.4%

시약·촉매·용매 2

HCID 2855718-Crown-6촉매HCID 6342Acetonitrile용매
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실험 절차

To a solution of compound 4-Fluorobenzenesulfonyl chloride (50 g, 0.256 mol) in ACN (500 mL) was added KF (74.36 g, 5 eq) and 18-crown-6 (2 g) at r.t., then the mixture was stirred at r.t. overnight. The mixture was detected by LC-MS, then saturated aqueous NaHCO3 was added and the mixture was extracted with EtOAc, the organic layer was washed with saturated aqueous NaHCO3, brine, dried over anhydrous Na2SO4, concentrated to give the crude compound 4-Fluorobenzenesulfonyl fluoride (46.70 g) as pale yellow oil which was used for the next step without further purification. ESI-MS (M+1): 179 calc. for C6H4F2O2S.

후처리

  1. extractionthe mixture was extracted with EtOAc
  2. washthe organic layer was washed with saturated aqueous NaHCO3, brine
  3. dry with materialdried over anhydrous Na2SO4
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-cad535deeb50482a815c092fc9f19b18
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440989B2

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