Acetic Acid → 1,1,1,2-Tetrafluoro-2-(trifluoromethyl)butane
반응식
[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]참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
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.
후처리
- customAfter the exothermic reaction
- distillationdistilled
- customto collect a fraction with a b.p. less than 100° C
- customThe distillate was separated from water
- dry with materialdried over calcium chloride
- distillationredistilled
출처 및 근거
- ORD 기록
- ord-e94057a53ccc4672b341d30bdf8bc77b
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06703533B1
반응 노트
불러오는 중…