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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Perfluorocyclopentene → 1H,2H-Octafluorocyclopentane

HRID 1457427
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HRID 1457427 반응식
[F:1][C:2]1([F:13])[C:6]([F:7])=[C:5]([F:8])[C:4]([F:10])([F:9])[C:3]1([F:12])[F:11]>[Pd]>[F:8][CH:5]1[C:4]([F:9])([F:10])[C:3]([F:11])([F:12])[C:2]([F:1])([F:13])[CH:6]1[F:7]
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참가 물질

3

반응물 1

HCID 11212Perfluorocyclopentene

생성물 1

HCID 27784261H,2H-Octafluorocyclopentane수율 99%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

Then a reactor was charged with 12 g of the octafluorocyclopentene and 0.24 g of a 5%-palladium/carbon catalyst and hydrogenation was conducted at a temperature of 50° C. and a hydrogenation pressure of 6 kg/cm2. When the absorption of hydrogen ceased, the reaction was completed. After the removal of the catalyst and the produced hydrogen fluoride from the reaction mixture, the reaction mixture was distilled to give 9 g of 1,2,3,3,4,4,5,5-octafluorocyclopentane (b.p., 79° C.; purity, 99%).

후처리

  1. customwas conducted at a temperature of 50° C.
  2. customWhen the absorption of hydrogen
  3. customAfter the removal of the catalyst
  4. distillationthe produced hydrogen fluoride from the reaction mixture, the reaction mixture was distilled

출처 및 근거

ORD 기록
ord-584f96472ccb4403bff642ff424fa547
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05847243

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