KR860008113A - 2,2,2- 트리플루오르에탄올의 제조방법 - Google Patents

2,2,2- 트리플루오르에탄올의 제조방법 Download PDF

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KR860008113A
KR860008113A KR1019860003104A KR860003104A KR860008113A KR 860008113 A KR860008113 A KR 860008113A KR 1019860003104 A KR1019860003104 A KR 1019860003104A KR 860003104 A KR860003104 A KR 860003104A KR 860008113 A KR860008113 A KR 860008113A
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catalyst
process according
formula
cocatalyst
compound
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KR1019860003104A
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KR910000773B1 (ko
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슈미날 베르나르
마때 앙리
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소시에떼 아토샹
미셀 로쉐
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/14Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/14Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
    • C07C29/141Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/34Halogenated alcohols
    • C07C31/40Halogenated alcohols perhalogenated

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

내용 없음

Description

2,2,2-트리플루오르에탄올의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (13)

  1. 하기 일반식(Ⅰ)의 화합물을 니켈촉매의 존재하에 액체상 촉매수소화하여 2,2,2,-트리플루오르에탄올을 제조하는 방법에 있어서, 지방족 3차 아민에서 선택된 공촉매의 존재하에 반응을 수행함을 특징으로 하는 방법.
    식중, R은 수소원자 또는 1∼8개의 탄소원자가 함유되고 임의로 부분플 적루오르화된 직쇄 또는 측쇄알킬 라디칼을 의미한다.
  2. 제1항에 있어서, 일반식(Ⅰ)의 화합물 및 공촉매의 혼합물을 물 또는 2,2,2-트리플루오르에탄올내에 현탁시킨 촉매의 현탁액에 점차로 도입하는 방법.
  3. 제1 또는 2항에 있어서, 반응종결 후에 반응혼합물을 신속히 냉각시키고, 촉매를 분리하여 다음 조작에 재사용하는 방법.
  4. 제3항에 있어서, 촉매를 여과분리한 후, 재사용전에 물로 세척하는 방법.
  5. 제3항에 있어서, 반응혼합물을 냉각시킨 후, 촉매를 침전시키고 반응액체를 배수시켜 반응기내에 남아있는 촉매를 재사용하는 방법.
  6. 제1 또는 2항에 있어서, 일반식(Ⅰ)의 화합물을 조상태로 사용하는 방법.
  7. 제1 또는 2항에 있어서, 조작을 150 내지 200℃, 바람직하게는 170 내지 180℃의 온도범위내에서 수행하는 방법.
  8. 제1 또는 2항에 있어서, 조작을 약 20 내지 50바아, 바람직하게는 30 내지 45바아의 압력내에서 수행하는 방법.
  9. 제1 또는 2항에 있어서, 촉매의 니켈함량이 30 내지 90 중량%, 바람직하게는 약 64%인 방법.
  10. 제1 또는 2항에 있어서, 촉매를 30 내지 45바아의 수소압 및 140 내지 200℃의 온도범위내에서 미리 활성화시키는 방법.
  11. 제1 또는 2항에 있어서, 64%의 니켈이 함유된 촉매의 경우, 촉매의 양이 사용된 수화물 또는 헤미아세탈의 중량에 대해 0.2 내지 7.5%, 바람직하게는 0.5 내지 2%인 방법.
  12. 제1 또는 2항에 있어서, 공촉매의 양인 일반식(Ⅰ)의 조화합물내에 존재하는 염소화된 부산물의 염소 그램-원자당 약 1.05 내지 6몰, 바람직하게는 1.05 내지 4몰인 방법.
  13. 제12항에 있어서, 공촉매가 일반식 R1-N(R2)R3의 아민인 방법.
    식중, R1,R2및R3는 동일하거나 또는 다르고, 각각은 히드록실기에 의해 임의로 치환된 알킬라디칼을 의미한다.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019860003104A 1985-04-23 1986-04-22 2,2,2-트리플루오로에탄올의 제조방법 KR910000773B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR8506121A FR2580630B1 (fr) 1985-04-23 1985-04-23 Procede de synthese du trifluoro-2,2,2 ethanol
FR8506121 1985-04-23
FR06121 1985-04-23

Publications (2)

Publication Number Publication Date
KR860008113A true KR860008113A (ko) 1986-11-12
KR910000773B1 KR910000773B1 (ko) 1991-02-06

Family

ID=9318543

Family Applications (1)

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KR1019860003104A KR910000773B1 (ko) 1985-04-23 1986-04-22 2,2,2-트리플루오로에탄올의 제조방법

Country Status (16)

Country Link
US (1) US4658070A (ko)
EP (1) EP0200621B1 (ko)
JP (1) JPS61249941A (ko)
KR (1) KR910000773B1 (ko)
AT (1) ATE32879T1 (ko)
AU (1) AU591114B2 (ko)
CA (1) CA1251468A (ko)
DE (1) DE3660032D1 (ko)
DK (1) DK184386A (ko)
ES (1) ES8704438A1 (ko)
FR (1) FR2580630B1 (ko)
GR (1) GR861048B (ko)
IE (1) IE58474B1 (ko)
IL (1) IL78561A0 (ko)
NO (1) NO162959C (ko)
ZA (1) ZA863035B (ko)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001068578A1 (fr) * 2000-03-14 2001-09-20 Daikin Industries, Ltd. Trifluoroacetaldehyde trifluoroethyle hemi-acetal et son procede de preparation
KR101364249B1 (ko) * 2006-04-28 2014-02-14 가부시키가이샤 구라레 3-메틸-1,5-펜탄디올의 제조 방법

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1229058B (de) * 1963-06-22 1966-11-24 Hoechst Ag Verfahren zur Herstellung von 1, 1, 1-Trifluoraethanol
JPS6059219B2 (ja) * 1981-11-18 1985-12-24 セントラル硝子株式会社 2−トリフルオロメチルプロパノ−ルの製造方法
GB8334566D0 (en) * 1983-12-29 1984-02-01 Ici Plc Chemical process
FR2567876B1 (fr) * 1984-07-18 1986-11-28 Atochem Procede de preparation des hydrates de fluoral et d'hexafluoroacetone purs a partir d'hemiacetals
FR2567875B1 (fr) * 1984-07-18 1986-08-08 Atochem Procede de synthese du trifluoro-2,2,2 ethanol et de l'alcool hexafluoro-1,1,1,3,3,3 isopropylique

Also Published As

Publication number Publication date
AU5647186A (en) 1986-10-30
US4658070A (en) 1987-04-14
ES8704438A1 (es) 1987-04-01
AU591114B2 (en) 1989-11-30
NO162959B (no) 1989-12-04
DE3660032D1 (en) 1988-04-14
IE861072L (en) 1986-10-23
EP0200621A1 (fr) 1986-11-05
ATE32879T1 (de) 1988-03-15
FR2580630B1 (fr) 1987-05-29
ES554243A0 (es) 1987-04-01
JPS6311334B2 (ko) 1988-03-14
DK184386D0 (da) 1986-04-22
KR910000773B1 (ko) 1991-02-06
GR861048B (en) 1986-08-12
NO162959C (no) 1990-03-14
IL78561A0 (en) 1986-08-31
NO861574L (no) 1986-10-24
JPS61249941A (ja) 1986-11-07
FR2580630A1 (fr) 1986-10-24
IE58474B1 (en) 1993-09-22
EP0200621B1 (fr) 1988-03-09
DK184386A (da) 1986-10-24
ZA863035B (en) 1986-12-30
CA1251468A (fr) 1989-03-21

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