JPH0564622B2 - - Google Patents
Info
- Publication number
- JPH0564622B2 JPH0564622B2 JP60016096A JP1609685A JPH0564622B2 JP H0564622 B2 JPH0564622 B2 JP H0564622B2 JP 60016096 A JP60016096 A JP 60016096A JP 1609685 A JP1609685 A JP 1609685A JP H0564622 B2 JPH0564622 B2 JP H0564622B2
- Authority
- JP
- Japan
- Prior art keywords
- styrene oxide
- phenylacetaldehyde
- catalyst
- reaction
- rate
- 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 - Lifetime
Links
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 claims description 38
- 238000006243 chemical reaction Methods 0.000 claims description 26
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 claims description 21
- 229940100595 phenylacetaldehyde Drugs 0.000 claims description 19
- 239000003054 catalyst Substances 0.000 claims description 18
- 238000009835 boiling Methods 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- 238000006317 isomerization reaction Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000006555 catalytic reaction Methods 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229940057995 liquid paraffin Drugs 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910002019 Aerosil® 380 Inorganic materials 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000008122 artificial sweetener Substances 0.000 description 1
- 235000021311 artificial sweeteners Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 1
- 229940044175 cobalt sulfate Drugs 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- -1 phenyl glycide ester Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60016096A JPS61176547A (ja) | 1985-01-30 | 1985-01-30 | フエニルアセトアルデヒドの製造法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60016096A JPS61176547A (ja) | 1985-01-30 | 1985-01-30 | フエニルアセトアルデヒドの製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61176547A JPS61176547A (ja) | 1986-08-08 |
JPH0564622B2 true JPH0564622B2 (pt) | 1993-09-16 |
Family
ID=11906981
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60016096A Granted JPS61176547A (ja) | 1985-01-30 | 1985-01-30 | フエニルアセトアルデヒドの製造法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61176547A (pt) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3632529A1 (de) * | 1986-09-25 | 1988-04-07 | Basf Ag | Verfahren zur herstellung von aldehyden und/oder ketonen durch umsetzung von epoxiden |
-
1985
- 1985-01-30 JP JP60016096A patent/JPS61176547A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61176547A (ja) | 1986-08-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5994595A (en) | Production process for (poly)alkylene glycol monoalkyl ether | |
KR20100059891A (ko) | 글리세롤로부터 아크롤레인을 제조하는 방법 | |
JP4744697B2 (ja) | フェノールの製造 | |
JP2003506342A (ja) | フェノール及びアセトンの製造方法 | |
KR102008526B1 (ko) | 제올라이트 성형체의 제조 방법 및 ε-카프로락탐의 제조 방법 | |
US4822921A (en) | Method for one-step synthesis of methyl t-butyl ether | |
JPH0564622B2 (pt) | ||
JPH0516418B2 (pt) | ||
JPH1135498A (ja) | クメンの製造方法 | |
US4299987A (en) | Process for producing benzo-phenone from 1,1-diphenylethane (or 1,1-diphenylethylene) using antimonate catalysts | |
JPS6312854B2 (pt) | ||
JPH0564623B2 (pt) | ||
JPH01113341A (ja) | カルボン酸メチルエステルの製造法 | |
JPH07119182B2 (ja) | アリールエチレングリコールの製造方法 | |
JPH01190639A (ja) | イソプロピルビフェニル類の製造方法 | |
JPH055820B2 (pt) | ||
US4528280A (en) | Process for preparing phosphorus-vanadium mixed oxide catalysts | |
US4515973A (en) | Process for producing maleic anhydride | |
JP3568293B2 (ja) | 2,3−ジメチル−2−ブテンの製造方法 | |
JPH04279557A (ja) | アゾメチン類の製造方法 | |
JP4489549B2 (ja) | 高純度2,2−ビス(3’−シクロヘキセニル)プロパンの製造方法 | |
JPH0517404A (ja) | ピルビン酸エステルの製造方法 | |
JPS6312455B2 (pt) | ||
JPS6239135B2 (pt) | ||
JPH0574579B2 (pt) |