Acetic Acid → 1,1,1,2-Tetrafluoro-2-(trifluoromethyl)butane

HRID 48544Notes

Reaction equation

HRID 48544 reaction equation
[C:1]([CH2:11][CH2:12]I)([C:7]([F:10])([F:9])[F:8])([C:3]([F:6])([F:5])[F:4])[F:2].C(O)(=O)C>O.[Zn]>[C:1]([CH2:11][CH3:12])([C:3]([F:4])([F:5])[F:6])([C:7]([F:10])([F:9])[F:8])[F:2]

Participants

5

Conditions

Temperature
60 °C

Procedure

A mixture of perfluoroisopropyl iodide (5.6 g, 0.19 mole), ethylene (5 L, 0.2 mole) and benzoyl peroxide (3.2 g) was heated in a 100 mL steel autoclave at 100° C. for 6 hours with stirring. The reaction product contained perfluoroisopropyl,iodide and (CF3)2CFCH2CH2I in a 1:1 ratio. Distillation of the reaction mixture gave (CF3)2CFCH2CH2I (b.p. 118 to 124° C.) in 33% yield. (CF3)2CFCH2CH2I (10 g) was added dropwise to a mixture of zinc dust (5 g) and acetic acid (30 mL). After the exothermic reaction was completed, the reaction mixture was stirred for 2.5 hours at 60° C., diluted with water and distilled to collect a fraction with a b.p. less than 100° C. The distillate was separated from water, dried over calcium chloride, and redistilled to give (CF3)2CFCH2CH3 (b.p. 39 to 42° C., 56% yield). The 1H and 19F NMR were in accord with the assigned structure.

Workup

  1. customAfter the exothermic reaction
  2. distillationdistilled
  3. customto collect a fraction with a b.p. less than 100° C
  4. customThe distillate was separated from water
  5. dry with materialdried over calcium chloride
  6. distillationredistilled

Sources & evidence

ORD record
ord-e94057a53ccc4672b341d30bdf8bc77b
Source dataset
uspto-grants-2004_03
Patent number
US06703533B1

Reaction notes

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