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Triethylamine → 1,1,2,2,3,3-Hexafluorocyclopentane

HRID 1199845
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HRID 1199845 반응식
Cl[C:2]1[C:6]([F:8])([F:7])[C:5]([F:10])([F:9])[C:4]([F:12])([F:11])[C:3]=1Cl.C(N(CC)CC)C>CO.[Ni]>[F:7][C:6]1([F:8])[CH2:2][CH2:3][C:4]([F:12])([F:11])[C:5]1([F:9])[F:10]
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참가 물질

5

반응물 2

HCID 8471TriethylamineHCID 128151,2-Dichloroperfluorocyclopentene

생성물 1

HCID 109975961,1,2,2,3,3-Hexafluorocyclopentane수율 60%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

In a 1.3 1 stainless steel autoclave, 245 g (1 mol) of 1,2-dichloro-3,3,4,4,5,5-hexafluorocyclopentene were hydrogenated at 60°to 70° C. with the addition of 202 g (2 mol) of triethylamine in 200 ml of methanol and in the presence of 20 g of Raney nickel. Over a period of 12 hours, the theoretical amount of hydrogen was absorbed at a hydrogen pressure of 40 to 50 bar. The reaction mixture was filtered and the methanolic solution was diluted with 400 ml of water. The lower organic phase was separated, washed with 100 ml of 5% aqueous hydrochloric acid, and dried over sodium sulfate. Distillation through a 1-m spinning band column gave 106 g (60% of theory) of 1,1,2,2,3,3-hexafluorocyclopentane having a boiling point of 87°-88° C. at 1013 mbar. The mass spectrum showed the molecular ion at m/e 178.

후처리

  1. customthe theoretical amount of hydrogen was absorbed at a hydrogen pressure of 40 to 50 bar
  2. filtrationThe reaction mixture was filtered
  3. additionthe methanolic solution was diluted with 400 ml of water
  4. customThe lower organic phase was separated
  5. washwashed with 100 ml of 5% aqueous hydrochloric acid
  6. dry with materialdried over sodium sulfate
  7. distillationDistillation through a 1-m

출처 및 근거

ORD 기록
ord-1577f0b32109474a86e971360c5af8c1
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04902839

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