JPS62129231A - ジイソプロピルカルビノ−ルの製造方法 - Google Patents
ジイソプロピルカルビノ−ルの製造方法Info
- Publication number
- JPS62129231A JPS62129231A JP26223485A JP26223485A JPS62129231A JP S62129231 A JPS62129231 A JP S62129231A JP 26223485 A JP26223485 A JP 26223485A JP 26223485 A JP26223485 A JP 26223485A JP S62129231 A JPS62129231 A JP S62129231A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- diisopropyl
- reaction
- temperature
- carbinol
- 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.)
- Granted
Links
- BAYAKMPRFGNNFW-UHFFFAOYSA-N 2,4-dimethylpentan-3-ol Chemical compound CC(C)C(O)C(C)C BAYAKMPRFGNNFW-UHFFFAOYSA-N 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 claims abstract description 74
- 239000003054 catalyst Substances 0.000 claims abstract description 55
- 229910052707 ruthenium Inorganic materials 0.000 claims abstract description 13
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims abstract description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 29
- 239000002994 raw material Substances 0.000 abstract description 21
- 239000013543 active substance Substances 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 4
- -1 extractants Substances 0.000 abstract description 3
- 239000003905 agrochemical Substances 0.000 abstract description 2
- 230000003197 catalytic effect Effects 0.000 abstract description 2
- 239000003814 drug Substances 0.000 abstract description 2
- 239000007791 liquid phase Substances 0.000 abstract description 2
- 239000003505 polymerization initiator Substances 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000007792 gaseous phase Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000002304 perfume Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 56
- 239000001257 hydrogen Substances 0.000 description 32
- 229910052739 hydrogen Inorganic materials 0.000 description 32
- 238000004817 gas chromatography Methods 0.000 description 23
- 238000010521 absorption reaction Methods 0.000 description 21
- 239000000243 solution Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000007868 Raney catalyst Substances 0.000 description 4
- 229910000564 Raney nickel Inorganic materials 0.000 description 4
- 239000012295 chemical reaction liquid Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000005909 Kieselgur Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000005674 electromagnetic induction Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- SXKJCXWNWBRZGB-UHFFFAOYSA-N chromium copper manganese Chemical compound [Mn][Cr][Cu] SXKJCXWNWBRZGB-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- QFVBCWBVMGRFQN-UHFFFAOYSA-N [Ba].[Cr].[Cu] Chemical compound [Ba].[Cr].[Cu] QFVBCWBVMGRFQN-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000011085 pressure filtration Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229910021484 silicon-nickel alloy Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 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
- C07C29/143—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 ketones
- C07C29/145—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 ketones with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26223485A JPS62129231A (ja) | 1985-11-21 | 1985-11-21 | ジイソプロピルカルビノ−ルの製造方法 |
EP19860308231 EP0227250B1 (en) | 1985-11-21 | 1986-10-22 | Process for producing diisopropylcarbinol |
DE8686308231T DE3678122D1 (de) | 1985-11-21 | 1986-10-22 | Herstellungsverfahren von diisopropylcarbinol. |
CN86107733.4A CN1003933B (zh) | 1985-11-21 | 1986-11-17 | 生产二异丙基甲醇的方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26223485A JPS62129231A (ja) | 1985-11-21 | 1985-11-21 | ジイソプロピルカルビノ−ルの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62129231A true JPS62129231A (ja) | 1987-06-11 |
JPH0513935B2 JPH0513935B2 (en, 2012) | 1993-02-23 |
Family
ID=17372938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26223485A Granted JPS62129231A (ja) | 1985-11-21 | 1985-11-21 | ジイソプロピルカルビノ−ルの製造方法 |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0227250B1 (en, 2012) |
JP (1) | JPS62129231A (en, 2012) |
CN (1) | CN1003933B (en, 2012) |
DE (1) | DE3678122D1 (en, 2012) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011034198A1 (ja) * | 2009-09-17 | 2011-03-24 | 住友化学株式会社 | 二重結合を有する化合物の製造方法 |
JP2015117199A (ja) * | 2013-12-18 | 2015-06-25 | 三菱瓦斯化学株式会社 | ジイソブチルケトンの水素化によるジイソブチルカルビノールの製造法 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101085804B1 (ko) * | 2004-03-29 | 2011-11-22 | 간토 가가꾸 가부시키가이샤 | 광학 활성 알코올의 제법 |
JP2022154988A (ja) * | 2021-03-30 | 2022-10-13 | 世紀東急工業株式会社 | 舗装補修用材料及び舗装補修用材料の製造方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5533464A (en) * | 1978-06-28 | 1980-03-08 | Sisas | Manufacture of 22methylpentanee2*44diol |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3055840A (en) * | 1958-01-13 | 1962-09-25 | Engelhard Ind Inc | Ruthenium-containing catalysts and methods of making said catalysts and increasing their activity |
-
1985
- 1985-11-21 JP JP26223485A patent/JPS62129231A/ja active Granted
-
1986
- 1986-10-22 EP EP19860308231 patent/EP0227250B1/en not_active Expired
- 1986-10-22 DE DE8686308231T patent/DE3678122D1/de not_active Expired - Lifetime
- 1986-11-17 CN CN86107733.4A patent/CN1003933B/zh not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5533464A (en) * | 1978-06-28 | 1980-03-08 | Sisas | Manufacture of 22methylpentanee2*44diol |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011034198A1 (ja) * | 2009-09-17 | 2011-03-24 | 住友化学株式会社 | 二重結合を有する化合物の製造方法 |
JP2015117199A (ja) * | 2013-12-18 | 2015-06-25 | 三菱瓦斯化学株式会社 | ジイソブチルケトンの水素化によるジイソブチルカルビノールの製造法 |
Also Published As
Publication number | Publication date |
---|---|
EP0227250B1 (en) | 1991-03-13 |
JPH0513935B2 (en, 2012) | 1993-02-23 |
EP0227250A1 (en) | 1987-07-01 |
CN86107733A (zh) | 1987-06-17 |
CN1003933B (zh) | 1989-04-19 |
DE3678122D1 (de) | 1991-04-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
EXPY | Cancellation because of completion of term |