KR960010597A - 클로로(플루오로)부탄의 하이드로플루오르화 방법 - Google Patents

클로로(플루오로)부탄의 하이드로플루오르화 방법 Download PDF

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KR960010597A
KR960010597A KR1019950029021A KR19950029021A KR960010597A KR 960010597 A KR960010597 A KR 960010597A KR 1019950029021 A KR1019950029021 A KR 1019950029021A KR 19950029021 A KR19950029021 A KR 19950029021A KR 960010597 A KR960010597 A KR 960010597A
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butane
fluoro
chloro
catalyst
hydrofluorination
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KR1019950029021A
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KR100363940B1 (ko
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페네트리우 파스칼
잔센스 프란신
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피. 안토니
솔베이(소시에떼 아노님)
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • C07C17/202Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
    • C07C17/206Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

일반식 C4H5ClxF5-x(여기서, x=1~5)의 클로로-(플루오로)부탄을 원소주기율 표 Ⅲa, Ⅳ;a, Ⅴa, Ⅴb와 Ⅵb족 금속의 유도체에서 선택한 촉매의 존재하에 플루오르화 수소로 하이드로플루오르화하는 방법.

Description

클로로(플루오로)부탄의 하이드로플루오르화 방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (13)

  1. 일반식 C4H5ClxF5-x(여기서, x=1~5)의 클로로-(플루오로)-부탄을 플루오르화 수소로 하이드로플루오르화하는 방법에 있어서, 하이드로플루오르화를 원소주기율 표 Ⅲa, Ⅳa, Ⅴa, Ⅴb 와 Ⅵb족 금속의 유도체에서 택한 촉매이 존재하에서 행함을 특징으로 하는 상기 방법.
  2. 제1항에 있어서, 촉매를 원소주기율표 Ⅳa 와 Ⅴa족 금속의 유도체에서 선택함을 특징으로 하는 방법.
  3. 제2항에 있어서, 촉매를 주석과 안티모니 유도체에서 선택함을 특징으로 하는 방법.
  4. 제1항 내지 제3항중 어느 한 항에 있어서, 촉매를 염화물, 플루오르화물과 클로로플루오르화물에서 선택함을 특징으로 하는 방법.
  5. 제4항에 있어서, 촉매가 오염화 안티모니임을 특징으로 하는 방법.
  6. 제1항 내지 제5항중 어느 한 항에 있어서, 촉매를 클로로(플루오로)부탄의 몰당 0.001~1몰의 촉매 비율로 사용함을 특징으로 하는 방법.
  7. 제1항 내지 제6항중 어느 한 항에 있어서, 사용된 플루오르화 수소와 클로로(플루오로)부탄의 몰비가 4대 25임을 특징으로 하는 방법.
  8. 제1항 내지 제7항중 어느 한 항에 있어서, 하이드로플루오르화를 50℃~150℃의 온도에서 행함을 특징으로하는 방법.
  9. 제1항내지 제8항중 어느 한 항에 있어서, 하이드로플루오르화를 2~40바아의 압력하에 액체상으로 행함을 특징으로 하는 방법.
  10. 제1항 내지 제9항중 어느 한 항에 있어서, 클로로(플루오로)-부탄을 일반식 CH3-CCl2F2-x-CH2-CClyF3y(여기서, x=0,1 또는 2, y=0,1,2 또는 3, x+y1)의 화합물에서 선택함을 특징으로 하는 방법.
  11. 제10항에 있어서, 클로로(플루오로)부탄을 1,1,3,3-테트라플루오로-1-클로로부탄, 1,3,3-트리플루오로-1,1-디클로로부탄과 1,1,3-트리플루오로-1,3-디클로로부탄에서 선택함을 특징으로 하는 방법.
  12. 제10항 또는 제11항에 있어서, 클로로(플루오로)-부탄을 염화비닐리덴과 플루오르화 수소를 반응시켜서 얻음을 특징으로 하는 방법.
  13. 1,1,1,3,3-펜타플루오로부탄을 제조하기 위한 제10항 내지 제12항중 어느 하나에 따른 방법의 용도.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950029021A 1994-09-05 1995-09-05 클로로(플루오로)부탄의하이드로플루오르화방법 KR100363940B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR94-10684 1994-09-05
FR9410684 1994-09-05
FR9410684A FR2724167B1 (fr) 1994-09-05 1994-09-05 Procede pour l'hydrofluoration de chloro (fluoro) butane

Publications (2)

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KR960010597A true KR960010597A (ko) 1996-04-20
KR100363940B1 KR100363940B1 (ko) 2003-01-29

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US (1) US5739406A (ko)
EP (1) EP0699649B1 (ko)
JP (2) JP3944254B2 (ko)
KR (1) KR100363940B1 (ko)
AT (1) ATE186289T1 (ko)
BR (1) BR9503889A (ko)
CA (1) CA2157211C (ko)
DE (1) DE69513111T2 (ko)
DK (1) DK0699649T3 (ko)
ES (1) ES2140615T3 (ko)
FR (1) FR2724167B1 (ko)
TW (1) TW298589B (ko)

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KR100379625B1 (ko) * 2000-08-05 2003-04-10 주식회사 세종소재 수소 정제용 게터

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FR2724167B1 (fr) * 1994-09-05 1996-11-29 Solvay Procede pour l'hydrofluoration de chloro (fluoro) butane
GB9518525D0 (en) * 1995-09-11 1995-11-08 Zeneca Ltd Novel process
FR2744442B1 (fr) * 1996-02-01 1998-02-27 Atochem Elf Sa Preparation du 1,1,1,3,3-pentachlorobutane et du 1,1,1,3,3,-pentafluorobutane
US6075172A (en) * 1996-09-03 2000-06-13 Zeneca Limited Chlorofluorohydrocarbon and process thereto
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FR2768717B1 (fr) * 1997-09-24 1999-11-12 Solvay Procede de separation de fluorure d'hydrogene de ses melanges avec un hydrofluoroalcane contenant de 3 a 6 atomes de carbone
KR100633784B1 (ko) * 1998-09-03 2006-10-16 솔베이 플루오르 운트 데리바테 게엠베하 1,1,1,3,3-펜타플루오로부탄의 정제
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FR2791975B1 (fr) * 1999-03-24 2001-07-27 Solvay Procede de separation de fluorure d'hydrogene des ses melanges avec du 1,1,1,3,3-pentafluorobutane et procede de fabrication de 1,1,1,3,3-pentafluorobutane
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JP4817572B2 (ja) * 1999-10-06 2011-11-16 ソルヴェイ(ソシエテ アノニム) 有機化合物の調製法及び助触媒の回収方法
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Publication number Priority date Publication date Assignee Title
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JP2006335770A (ja) 2006-12-14
DE69513111T2 (de) 2000-08-17
ATE186289T1 (de) 1999-11-15
FR2724167A1 (fr) 1996-03-08
EP0699649B1 (fr) 1999-11-03
TW298589B (ko) 1997-02-21
BR9503889A (pt) 1996-09-17
JPH0899918A (ja) 1996-04-16
FR2724167B1 (fr) 1996-11-29
ES2140615T3 (es) 2000-03-01
DE69513111D1 (de) 1999-12-09
KR100363940B1 (ko) 2003-01-29
JP3944254B2 (ja) 2007-07-11
CA2157211A1 (fr) 1996-03-06
EP0699649A1 (fr) 1996-03-06
CA2157211C (fr) 2007-08-21
US5739406A (en) 1998-04-14
DK0699649T3 (da) 2000-05-08

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