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Allyl bromide → 4,4,5,5,6,6,7,7,7-Nonafluoro-1-heptene

HRID 963587
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HRID 963587 반응식
[F:1][C:2](I)([F:13])[C:3]([F:12])([F:11])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6].[CH2:15](Br)[CH:16]=[CH2:17]>[Cu].CS(C)=O>[F:1][C:2]([F:13])([C:3]([F:12])([F:11])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6])[CH2:17][CH:16]=[CH2:15]
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참가 물질

5

반응물 2

HCID 7841Allyl bromideHCID 67917Perfluorobutyl iodide

생성물 1

HCID 115797784,4,5,5,6,6,7,7,7-Nonafluoro-1-heptene수율 70.7%

시약·촉매·용매 2

HCID 23978Copper촉매HCID 679Dimethyl Sulfoxide용매

실험 절차

A mixture of perfluorobutyl iodide (103.8 g, 0.3 mol), copper powder (50 g, 0.79 mol) and dimethyl sulfoxide (150 mL) was stirred at 110°-120° C. for 2 hr, then cooled to room temperature. Allyl bromide (36.3 g, 0.3 mol) was added dropwise and then the mixture was stirred at room temperature for 2 hr and at 50° C. for 1 hr. The reaction mixture was distilled in vacuo and the crude product was collected in a cold trap (-78° C.). Redistillation produced 55.2 g (70% yield) of the desired 4,4,5,5,6,6,7,7,7-nonafluoro-1-heptene, formula above, having a boiling point of 79°-80° C.

후처리

  1. stirringthe mixture was stirred at room temperature for 2 hr and at 50° C. for 1 hr
  2. distillationThe reaction mixture was distilled in vacuo
  3. customthe crude product was collected in a cold trap (-78° C.)
  4. distillationRedistillation

출처 및 근거

ORD 기록
ord-1d1b9226f3454e558aa674478fc26520
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05763552

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