KR830007496A - 불포화산 및 에스테르의 제조방법 - Google Patents
불포화산 및 에스테르의 제조방법 Download PDFInfo
- Publication number
- KR830007496A KR830007496A KR1019810003303A KR810003303A KR830007496A KR 830007496 A KR830007496 A KR 830007496A KR 1019810003303 A KR1019810003303 A KR 1019810003303A KR 810003303 A KR810003303 A KR 810003303A KR 830007496 A KR830007496 A KR 830007496A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- catalyst
- compound
- base letter
- esters
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 239000002253 acid Substances 0.000 title 1
- 150000007513 acids Chemical class 0.000 title 1
- 150000002148 esters Chemical class 0.000 title 1
- 238000000034 method Methods 0.000 claims 10
- 239000003054 catalyst Substances 0.000 claims 3
- 229910052788 barium Inorganic materials 0.000 claims 2
- 229910052791 calcium Inorganic materials 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims 2
- 229910052749 magnesium Inorganic materials 0.000 claims 2
- 229910052715 tantalum Inorganic materials 0.000 claims 2
- 229910052716 thallium Inorganic materials 0.000 claims 2
- 229910052719 titanium Inorganic materials 0.000 claims 2
- 229910052725 zinc Inorganic materials 0.000 claims 2
- 229910052726 zirconium Inorganic materials 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 229910052684 Cerium Inorganic materials 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- 229910052793 cadmium Inorganic materials 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 229910001882 dioxygen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids
- C07C57/04—Acrylic acid; Methacrylic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/377—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 다음 구조식(Ⅱ)의 화합물을 분자상 산소의 존재하에서 촉매적 분량의 구조식(Ⅰ)의 촉매와 접촉시켜 다음 일반식(Ⅲ)의 화합물을 제조하는 증기상 공정.Mo12P0.1~2Bi0.01~3M0.1~3Cu0.01~2V0.01~3XaM'bOc(Ⅰ)상기구조식에서R~ R'''는 독립적으로 수소 또는 C1-C4알킬기를 나타내며 ;,M은 K, Rb 및 Cs 중 적어도 한가지이며 ;X는 a 〉0일때 Ba, Zn,Ga, Cd 및 Ti중 적어도 한가지이고 ;M'는 b 〉0일때 Ca, Mg, Ta, Zr, Ce, Ni, Co, Cr, Fe 및 Tl 중 적어도 한가지이며 ;a는 0 내지 약 2이고 ;b는 0 내지 약 2이며 ;c는 구조식내에 존재하는 다른 원소들과의 균형을 이루는데 필요한 원자가이다.
- 제1항에 있어서, a 〉0인 방법.
- 제2항에 있어서, M이 K 또는 Rb인 방법.
- 제3항에 있어서, X가 Ba, Zn, Cd 또는 Ti인 방법.
- 제4항에 있어서, b가 0인 방법.
- 제4항에 있어서, b 〉0인 방법.
- 제6항에 있어서, M'가 Ca, Mg, Tl, Ta 또는 Zr인 방법.
- 제5항에 있어서, 구조식(Ⅰ)에서 P의 밑 글자가 약 0.8 내지 약 1.5이고, Bi의 밑글자가 약 0.15 내지 1이며, M의 밑 글자가 약 0.1 내지 2이고, Cu의 밑글자가 약 0.2 내지 0.8이며, V의 밑글자가 약 0.2 내지 0.8인 방법.
- 제8항에 있어서, 촉매가 거의 100% 활성 형태인 방법.
- 제8항에 있어서, 촉매를 지지체로 희석하는 방법.
- 제10항에 있어서, 지지체가 저표면적 알루미나인 방법.
- 제10항에 있어서, 구조식(Ⅱ)의 화합물이 이소부티르산인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US184591 | 1980-09-05 | ||
US06/184,591 US4307247A (en) | 1980-09-05 | 1980-09-05 | Process for the production of unsaturated acids and esters |
US184,591 | 1980-09-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830007496A true KR830007496A (ko) | 1983-10-21 |
KR870001317B1 KR870001317B1 (ko) | 1987-07-13 |
Family
ID=22677541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019810003303A KR870001317B1 (ko) | 1980-09-05 | 1981-09-04 | 산 및 에스테르의 제조방법 |
Country Status (6)
Country | Link |
---|---|
US (1) | US4307247A (ko) |
EP (1) | EP0047578B1 (ko) |
JP (1) | JPS5750939A (ko) |
KR (1) | KR870001317B1 (ko) |
CA (1) | CA1150732A (ko) |
DE (1) | DE3163879D1 (ko) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4471062A (en) * | 1979-12-27 | 1984-09-11 | The Standard Oil Company | Method for the reactivation of deactivated phosphomolybdic acid based catalysts |
US4471061A (en) * | 1979-12-31 | 1984-09-11 | The Standard Oil Company | Methods for treatment of phosphomolybdic acid based catalysts during reactor shutdown |
DE3161102D1 (en) * | 1980-08-28 | 1983-11-10 | Roehm Gmbh | Process for the oxidizing dehydrogenation of isobutyric acid to methacrylic acid |
US4391989A (en) * | 1981-11-09 | 1983-07-05 | Ashland Oil, Inc. | Oxydehydrogenation of isobutyric acid and its lower alkyl esters |
DE3145091A1 (de) * | 1981-11-13 | 1983-05-19 | Röhm GmbH, 6100 Darmstadt | Verfahren zur herstellung von methacrylsaeure |
US4788173A (en) * | 1985-12-20 | 1988-11-29 | The Standard Oil Company | Catalytic mixtures for ammoxidation of paraffins |
US4783545A (en) * | 1985-12-20 | 1988-11-08 | The Standard Oil Company | Method for ammoxidation of paraffins and catalyst system therefor |
KR0144645B1 (ko) * | 1994-12-26 | 1998-07-15 | 황선두 | 메타크릴산 제조용 촉매 |
US6693059B2 (en) * | 2000-02-09 | 2004-02-17 | Rohm And Haas Company | Process for preparing a catalyst and catalytic oxidation therewith |
US6534435B1 (en) * | 2001-09-26 | 2003-03-18 | Council Of Scientific And Industrial Research | Process for in situ synthesis of supported heteropoly acids and salts thereof |
KR20080053306A (ko) * | 2005-09-23 | 2008-06-12 | 이스트만 케미칼 컴파니 | 카르복시산 혼합물로부터 혼합형 케톤을 제조하기 위한선택적인 촉매 |
KR100915078B1 (ko) * | 2006-12-01 | 2009-09-02 | 주식회사 엘지화학 | 신규한 헤테로폴리산계 촉매 및 이의 제조방법 |
KR100954049B1 (ko) * | 2007-06-13 | 2010-04-20 | 주식회사 엘지화학 | 헤테로폴리산계 촉매의 제조방법 |
JP6452169B2 (ja) * | 2016-09-14 | 2019-01-16 | 日本化薬株式会社 | アクリル酸製造用触媒ならびにアクリル酸の製造方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4819614B1 (ko) * | 1970-11-30 | 1973-06-14 | ||
US3917673A (en) * | 1973-10-26 | 1975-11-04 | Eastman Kodak Co | Catalytic process for the manufacture of unsaturated acids and esters |
DE2550979C2 (de) * | 1975-11-13 | 1984-06-07 | Röhm GmbH, 6100 Darmstadt | Verfahren zur Herstellung von Methacrylsäure durch oxydative Dehydrierung von Isobuttersäure |
US4061673A (en) * | 1976-07-30 | 1977-12-06 | Mitsubishi Chemical Industries Ltd. | Manufacture of methacrylic acid |
YU41495B (en) * | 1979-01-23 | 1987-08-31 | Nippon Kayaku Kk | Process for obtaining methacrolein and methacrylic acid |
US4232174A (en) * | 1979-03-28 | 1980-11-04 | E. I. Du Pont De Nemours And Company | Catalyst and dehydrogenation process |
-
1980
- 1980-09-05 US US06/184,591 patent/US4307247A/en not_active Expired - Lifetime
-
1981
- 1981-06-03 CA CA000378937A patent/CA1150732A/en not_active Expired
- 1981-07-17 JP JP56112911A patent/JPS5750939A/ja active Pending
- 1981-07-24 EP EP81303409A patent/EP0047578B1/en not_active Expired
- 1981-07-24 DE DE8181303409T patent/DE3163879D1/de not_active Expired
- 1981-09-04 KR KR1019810003303A patent/KR870001317B1/ko active
Also Published As
Publication number | Publication date |
---|---|
CA1150732A (en) | 1983-07-26 |
KR870001317B1 (ko) | 1987-07-13 |
EP0047578B1 (en) | 1984-05-30 |
US4307247A (en) | 1981-12-22 |
JPS5750939A (en) | 1982-03-25 |
EP0047578A1 (en) | 1982-03-17 |
DE3163879D1 (en) | 1984-07-05 |
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