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

HRID 945

반응식

HRID 945 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]

참가 물질

6

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 flitrate was dissolved in methylene chloride (100 mL), washed with 1N HCl (50 mL), brine, and dried over anhydrous magnesinm 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 flitrate
  5. washwashed with 1N HCl (50 mL), brine
  6. dry with materialdried over anhydrous magnesinm sulfate
  7. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-cc001eb75d5743259d85df36a16ea38b
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05723470

연결된 노트

불러오는 중…