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Isopropanol → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

HRID 439673
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HRID 439673 반응식
[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5][OH:6].CC(C)=[O:13].OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C>CC(C)=O.C(Cl)Cl>[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][C:5]([OH:13])=[O:6]
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참가 물질

6

반응물 3

HCID 3776IsopropanolHCID 218364774-Bromo-3-chloro-3,4,4-trifluorobutan-1-olHCID 131709961Jones' reagent

생성물 1

HCID 109121274-Bromo-3-chloro-3,4,4-trifluorobutanoic acid수율 85%

시약·촉매·용매 2

HCID 180Acetone용매HCID 6344Dichloromethane
용매

실험 절차

A solution of 4-bromo-3-chloro-3,4,4-trifluorobutanol (IX) (2.41 g, 10 mmol) in acetone (35 mL) was treated with Jones reagent (7.5 mL) in 10 min with stirring and cooling (ice-water bath). The mixture was then stirred at room temperature for 30 min and 0.5 mL of i-propanol was then added. The precipitated salts were removed by filtration, washed with acetone. The residue obtained after concentration of the filtrate was dissolved in methylene chloride (100 mL), washed with 1N HCl (50 mL), brine, and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave 2.17 g (85%) of 4-bromo-3-chloro-3,4,4-trifluorobutanoic acid (VIII) as a clear oil.

후처리

  1. stirringThe mixture was then stirred at room temperature for 30 min
  2. customThe precipitated salts were removed by filtration
  3. washwashed with acetone
  4. customThe residue obtained after concentration of the filtrate
  5. washwashed with 1N HCl (50 mL), brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-77eaa78347e14d699c10a4101f11b5b8
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05514717

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