تفاعل #1041

ord-cc001eb75d5743259d85df36a16ea38b

معادلة التفاعل

CC(C)O
i-propanol
OCCC(F)(Cl)C(F)(F)Br
4-bromo-3-chloro-3,4,4-trifluorobutanol
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
O=C(O)CC(F)(Cl)C(F)(F)Br
4-bromo-3-chloro-3,4,4-trifluorobutanoic acid
المردود 85.0%
O=C(O)CC(F)(Cl)C(F)(F)Br
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
المردود 85.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was then stirred at room temperature for 30 min
  2. 2
    أخرىThe precipitated salts were removed by filtration
  3. 3
    غسيلwashed with acetone
  4. 4
    أخرىThe residue obtained after concentration of the flitrate
  5. 5
    غسيلwashed with 1N HCl (50 mL), brine
  6. 6
    تجفيفdried over anhydrous magnesinm sulfate
  7. 7
    أخرىEvaporation of the solvent

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723470uspto-grants-1998_03