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Potassium Carbonate → 2-Fluoro-6-nitrophenyl Trifluoromethanesulfonate

HRID 620713
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HRID 620713 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-:10])=[O:9])[C:3]=1[OH:11].C(=O)([O-])[O-].[K+].[K+].[F:18][C:19]([F:25])([F:24])[S:20](Cl)(=[O:22])=[O:21]>CC(C)=O>[F:18][C:19]([F:25])([F:24])[S:20]([O:11][C:3]1[C:4]([N+:8]([O-:10])=[O:9])=[CH:5][CH:6]=[CH:7][C:2]=1[F:1])(=[O:22])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 737102-Fluoro-6-nitrophenolHCID 79000Trifluoromethanesulfonyl chloride

생성물 1

HCID 200290852-Fluoro-6-nitrophenyl Trifluoromethanesulfonate수율 53.1%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

A mixture consisting of 2-fluoro-6-nitrophenol (20 g, 0.14 mol) and potassium carbonate (20 g, 0.14 mol) in acetone (350 mL) was stirred at room temperature for 20 minutes. A solution of trifluoromethanesulfonyl chloride (23.7 g, 0.14 mol) in acetone (100 mL) was added dropwise at room temperature. Stirring was continued for 3 hours. The reaction was filtered, and the filtrate was concentrated. The residue was dissolved in diethyl ether (300 mL), washed with 0.1N NaOH, water, dried (MgSO4), filtered and evaporated to give 21.5 g of the title compound.

후처리

  1. stirringStirring
  2. waitwas continued for 3 hours
  3. filtrationThe reaction was filtered
  4. concentrationthe filtrate was concentrated
  5. dissolutionThe residue was dissolved in diethyl ether (300 mL)
  6. washwashed with 0.1N NaOH, water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customevaporated

출처 및 근거

ORD 기록
ord-dd02b2c4881548f0bc431b8c417f16fb
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04822781

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