JPS6240345B2 - - Google Patents
Info
- Publication number
- JPS6240345B2 JPS6240345B2 JP59089572A JP8957284A JPS6240345B2 JP S6240345 B2 JPS6240345 B2 JP S6240345B2 JP 59089572 A JP59089572 A JP 59089572A JP 8957284 A JP8957284 A JP 8957284A JP S6240345 B2 JPS6240345 B2 JP S6240345B2
- Authority
- JP
- Japan
- Prior art keywords
- yield
- acid
- reaction
- metal
- trifluoroacetic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003054 catalyst Substances 0.000 claims abstract description 19
- 239000010948 rhodium Substances 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 239000002253 acid Substances 0.000 claims abstract description 10
- 229910052703 rhodium Inorganic materials 0.000 claims abstract description 10
- 150000001768 cations Chemical class 0.000 claims abstract description 9
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 9
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000654 additive Substances 0.000 claims abstract description 7
- 230000000996 additive effect Effects 0.000 claims abstract description 6
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- -1 halide anions Chemical class 0.000 claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 48
- 238000006243 chemical reaction Methods 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 229910052745 lead Inorganic materials 0.000 claims description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
- 229910052715 tantalum Inorganic materials 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052707 ruthenium Inorganic materials 0.000 abstract description 6
- 229910052741 iridium Inorganic materials 0.000 abstract description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 abstract description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 230000000737 periodic effect Effects 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 20
- 239000007789 gas Substances 0.000 description 11
- 238000004458 analytical method Methods 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000010949 copper Substances 0.000 description 7
- QCUOBSQYDGUHHT-UHFFFAOYSA-L cadmium sulfate Chemical compound [Cd+2].[O-]S([O-])(=O)=O QCUOBSQYDGUHHT-UHFFFAOYSA-L 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 5
- 229910000331 cadmium sulfate Inorganic materials 0.000 description 5
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 239000012429 reaction media Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- PBCFLUZVCVVTBY-UHFFFAOYSA-N tantalum pentoxide Chemical compound O=[Ta](=O)O[Ta](=O)=O PBCFLUZVCVVTBY-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000004868 gas analysis Methods 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 3
- 238000010517 secondary reaction Methods 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229940076286 cupric acetate Drugs 0.000 description 2
- 229940046892 lead acetate Drugs 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- MINVSWONZWKMDC-UHFFFAOYSA-L mercuriooxysulfonyloxymercury Chemical compound [Hg+].[Hg+].[O-]S([O-])(=O)=O MINVSWONZWKMDC-UHFFFAOYSA-L 0.000 description 1
- 229910000371 mercury(I) sulfate Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 1
- 229910000367 silver sulfate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910000375 tin(II) sulfate Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation 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
- C07C29/136—Preparation 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
- C07C29/147—Preparation 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 carboxylic acids or derivatives thereof
- C07C29/149—Preparation 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 carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8307569A FR2545481B1 (fr) | 1983-05-06 | 1983-05-06 | Procede de preparation de perfluoroalcanols |
| FR8307569 | 1983-05-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS604143A JPS604143A (ja) | 1985-01-10 |
| JPS6240345B2 true JPS6240345B2 (forum.php) | 1987-08-27 |
Family
ID=9288653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59089572A Granted JPS604143A (ja) | 1983-05-06 | 1984-05-07 | ペルフルオルアルカノ−ルの製造方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4590309A (forum.php) |
| EP (1) | EP0128059B1 (forum.php) |
| JP (1) | JPS604143A (forum.php) |
| AT (1) | ATE20048T1 (forum.php) |
| BR (1) | BR8402097A (forum.php) |
| CA (1) | CA1221387A (forum.php) |
| DE (1) | DE3460176D1 (forum.php) |
| ES (1) | ES532174A0 (forum.php) |
| FR (1) | FR2545481B1 (forum.php) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0614590U (ja) * | 1992-07-31 | 1994-02-25 | 三ツ星ベルト株式会社 | 極薄平ベルト |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2612178B1 (fr) * | 1987-03-12 | 1989-07-21 | Inst Francais Du Petrole | Procede de fabrication d'alcools par hydrogenolyse d'esters d'acides carboxyliques en presence d'un catalyseur contenant du ruthenium et de l'etain, du germanium ou du plomb |
| FR2638158B1 (fr) * | 1988-10-21 | 1991-04-12 | Rhone Poulenc Chimie | Procede de preparation de trifluoroethanol |
| US20040030199A1 (en) * | 2002-01-29 | 2004-02-12 | Maughon Robert R. | Process for reducing alpha-haloketones to secondary alpha-haloalcohols |
| CN104829432B (zh) * | 2015-03-18 | 2017-02-01 | 武汉工程大学 | 一种制备氟代醇的方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2862977A (en) * | 1956-12-21 | 1958-12-02 | Du Pont | Hydrogenation of perfluoroalkanoic acids to 1, 1-dihydroperfluoroalkyl alcohols over ruthenium catalyst |
| NL135676C (forum.php) * | 1960-10-17 | |||
| US3390191A (en) * | 1964-03-24 | 1968-06-25 | Allied Chem | Hydrogenation of methyl trifluoroacetate to trifluoroethanol |
| BE755624A (fr) * | 1969-09-02 | 1971-03-02 | Hoechst Ag | Procede de preparation de 1,1-dihydro-perfluoro-alcanols |
| DE2222682A1 (de) * | 1972-05-09 | 1973-11-22 | Hoechst Ag | Verfahren zur hydrierung von perfluoralkancarbonsaeuren |
| US4273947A (en) * | 1979-01-31 | 1981-06-16 | Allied Chemical Corporation | Hydrogenation of fluorine-containing carboxylic acids |
| US4396784A (en) * | 1980-06-24 | 1983-08-02 | Phillips Petroleum Company | Hydrogenation of fluoroacids with rhenium-fluorided alumina catalyst |
-
1983
- 1983-05-06 FR FR8307569A patent/FR2545481B1/fr not_active Expired
-
1984
- 1984-04-27 DE DE8484400856T patent/DE3460176D1/de not_active Expired
- 1984-04-27 AT AT84400856T patent/ATE20048T1/de not_active IP Right Cessation
- 1984-04-27 EP EP84400856A patent/EP0128059B1/fr not_active Expired
- 1984-05-04 ES ES532174A patent/ES532174A0/es active Granted
- 1984-05-04 BR BR8402097A patent/BR8402097A/pt unknown
- 1984-05-04 CA CA000453589A patent/CA1221387A/fr not_active Expired
- 1984-05-07 JP JP59089572A patent/JPS604143A/ja active Granted
-
1985
- 1985-04-30 US US06/727,621 patent/US4590309A/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0614590U (ja) * | 1992-07-31 | 1994-02-25 | 三ツ星ベルト株式会社 | 極薄平ベルト |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0128059A3 (en) | 1985-01-09 |
| US4590309A (en) | 1986-05-20 |
| EP0128059A2 (fr) | 1984-12-12 |
| FR2545481B1 (fr) | 1985-07-19 |
| BR8402097A (pt) | 1984-12-11 |
| ES8502073A1 (es) | 1984-12-16 |
| JPS604143A (ja) | 1985-01-10 |
| DE3460176D1 (en) | 1986-07-03 |
| ATE20048T1 (de) | 1986-06-15 |
| FR2545481A1 (fr) | 1984-11-09 |
| CA1221387A (fr) | 1987-05-05 |
| EP0128059B1 (fr) | 1986-05-28 |
| ES532174A0 (es) | 1984-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE68907808T2 (de) | Hydrodehalogenierung von 1,1,1,2-Tetrafluorchlorethan in Gegenwart von auf einem Träger aufgebrachtem Palladium. | |
| EA017145B1 (ru) | Способ превращения углеводородов в этанол | |
| JPH0457655B2 (forum.php) | ||
| US4152352A (en) | Process for the carbonylation of aralkylhalides | |
| JPH06256235A (ja) | １，１，１，３，３−ペンタフルオロプロパンの製造方法 | |
| JPS6240345B2 (forum.php) | ||
| JPS646183B2 (forum.php) | ||
| US4126752A (en) | Homologation of methanol with a carbon monoxide-water mixture | |
| JP2001240569A (ja) | −ｃｈ２−ｃｈｆ−基を有する化合物の製造方法 | |
| JP2757885B2 (ja) | 炭酸ジエステルの製造法 | |
| JPS60208945A (ja) | 第２のエステルの製造方法 | |
| EP1127865B1 (en) | Process for producing 1,1,1-Trifluoroacetone | |
| JP2650100B2 (ja) | エチリデンジアセテートの製造方法 | |
| JPS58121226A (ja) | エチレン・グリコ−ル及び低級１価アルコ−ルの製造方法 | |
| JPH0125729B2 (forum.php) | ||
| US4533771A (en) | Process for the preparation of trifluoroethanol | |
| US5602288A (en) | Catalytic process for producing CF3 CH2 F | |
| JP2004091368A (ja) | 含ハロゲンアルコールおよびその製造方法 | |
| JP2003089666A (ja) | ハロゲン化アルコ−ルの製造方法 | |
| JPH0688919B2 (ja) | 含水素フルオロクロロアルカンの製造方法 | |
| JPH05140009A (ja) | １，１，１，２，２，３，４，５，５，５−デカフルオロペンタンの製造方法 | |
| EP0149905A2 (en) | Method for the preparation of 2,2,2-trifluoroethanol | |
| JP4099630B2 (ja) | パーフルオロアルキル化合物の製造方法 | |
| JP4136318B2 (ja) | １，３−ジフルオロアセトンの製造方法 | |
| CN106518646A (zh) | 一种通过甲酸甲酯异构化制备乙酸的方法 |