JPS5815935A - ベンズアルデヒド類の製造法 - Google Patents
ベンズアルデヒド類の製造法Info
- Publication number
- JPS5815935A JPS5815935A JP56112977A JP11297781A JPS5815935A JP S5815935 A JPS5815935 A JP S5815935A JP 56112977 A JP56112977 A JP 56112977A JP 11297781 A JP11297781 A JP 11297781A JP S5815935 A JPS5815935 A JP S5815935A
- Authority
- JP
- Japan
- Prior art keywords
- chloride
- acid
- catalyst
- reaction
- benzal
- 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
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 title abstract description 10
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 title abstract description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 38
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical compound ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000002253 acid Substances 0.000 claims abstract description 17
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 12
- 230000007062 hydrolysis Effects 0.000 claims abstract description 11
- 125000005843 halogen group Chemical group 0.000 claims abstract description 4
- 150000003935 benzaldehydes Chemical class 0.000 claims description 15
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 23
- 239000003054 catalyst Substances 0.000 abstract description 21
- 230000000694 effects Effects 0.000 abstract description 10
- 239000002994 raw material Substances 0.000 abstract description 10
- 230000003301 hydrolyzing effect Effects 0.000 abstract description 7
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract description 4
- 229910000040 hydrogen fluoride Inorganic materials 0.000 abstract description 4
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 239000012808 vapor phase Substances 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000000034 method Methods 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 11
- 239000007789 gas Substances 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 6
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 6
- 125000006575 electron-withdrawing group Chemical group 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- -1 trifluoro-substituted benzal chloride Chemical class 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000006200 vaporizer Substances 0.000 description 4
- 150000001805 chlorine compounds Chemical group 0.000 description 3
- 229960003280 cupric chloride Drugs 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- QMRLRZLQIJAGSQ-UHFFFAOYSA-N 1,3-dibromo-2-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=C(Br)C=CC=C1Br QMRLRZLQIJAGSQ-UHFFFAOYSA-N 0.000 description 1
- QQPXXHAEIGVZKQ-UHFFFAOYSA-N 1,3-dichloro-2-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=C(Cl)C=CC=C1Cl QQPXXHAEIGVZKQ-UHFFFAOYSA-N 0.000 description 1
- NDNNQDFCSZTPBG-UHFFFAOYSA-N 1,4-dibromo-2-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC(Br)=CC=C1Br NDNNQDFCSZTPBG-UHFFFAOYSA-N 0.000 description 1
- VBPLROSJWVETJQ-UHFFFAOYSA-N 1,4-dichloro-2-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC(Cl)=CC=C1Cl VBPLROSJWVETJQ-UHFFFAOYSA-N 0.000 description 1
- XFAFBKQDEPXWCS-UHFFFAOYSA-N 1-(dichloromethyl)-2-fluorobenzene Chemical compound FC1=CC=CC=C1C(Cl)Cl XFAFBKQDEPXWCS-UHFFFAOYSA-N 0.000 description 1
- MVRCPAOYPLZMLB-UHFFFAOYSA-N 1-(dichloromethyl)-3-fluorobenzene Chemical compound FC1=CC=CC(C(Cl)Cl)=C1 MVRCPAOYPLZMLB-UHFFFAOYSA-N 0.000 description 1
- MFIOEEWGBMJNGG-UHFFFAOYSA-N 1-(dichloromethyl)-4-fluorobenzene Chemical compound FC1=CC=C(C(Cl)Cl)C=C1 MFIOEEWGBMJNGG-UHFFFAOYSA-N 0.000 description 1
- PQYGNIRJOCANCU-UHFFFAOYSA-N 1-bromo-4-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC=C(Br)C=C1 PQYGNIRJOCANCU-UHFFFAOYSA-N 0.000 description 1
- VWHNJDGWDOQJRM-UHFFFAOYSA-N 1-chloro-4-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC=C(Cl)C=C1 VWHNJDGWDOQJRM-UHFFFAOYSA-N 0.000 description 1
- XQAYFQKXUOLNPQ-UHFFFAOYSA-N 2,4-dibromo-1-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC=C(Br)C=C1Br XQAYFQKXUOLNPQ-UHFFFAOYSA-N 0.000 description 1
- AQVKVGOTPBBVMS-UHFFFAOYSA-N 2,4-dichloro-1-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=CC=C(Cl)C=C1Cl AQVKVGOTPBBVMS-UHFFFAOYSA-N 0.000 description 1
- SRWILAKSARHZPR-UHFFFAOYSA-N 3-chlorobenzaldehyde Chemical compound ClC1=CC=CC(C=O)=C1 SRWILAKSARHZPR-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 150000005524 benzylchlorides Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56112977A JPS5815935A (ja) | 1981-07-21 | 1981-07-21 | ベンズアルデヒド類の製造法 |
| GB08218612A GB2103208B (en) | 1981-07-21 | 1982-06-28 | Vapor phase catalytic hydrolysis of benzal chloride or its halogen- or trifluoromethyl-substitute to form benzaldehyde or substitute |
| IT22211/82A IT1157289B (it) | 1981-07-21 | 1982-07-02 | Idrolisi catalitica in fas vapore di cloruro di benzale o il suo alogeno o trifluorometil-sostituto per formare benzaldeide o sostituto |
| DE3226490A DE3226490C2 (de) | 1981-07-21 | 1982-07-15 | Verfahren zur Herstellung von Benzaldehyd oder dessen Halogen- oder Trifluormethylverbindungen durch katalytische Dampfphasenhydrolyse von Benzalchlorid oder den entsprechend substituierten Verbindungen |
| FR8212665A FR2510101B1 (fr) | 1981-07-21 | 1982-07-20 | Procede d'hydrolyse catalytique en phase vapeur de chlorure de benzal ou son substitut avec un halogene ou un trifluoromethyle, pour former du benzaldehyde ou son substitut |
| US06/400,011 US4450298A (en) | 1981-07-21 | 1982-07-20 | Vapor phase catalytic hydrolysis of benzal chloride or its halogen- or trifluoromethyl-substitute to form benzaldehyde or substitute |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56112977A JPS5815935A (ja) | 1981-07-21 | 1981-07-21 | ベンズアルデヒド類の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5815935A true JPS5815935A (ja) | 1983-01-29 |
| JPS629576B2 JPS629576B2 (enrdf_load_stackoverflow) | 1987-02-28 |
Family
ID=14600299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56112977A Granted JPS5815935A (ja) | 1981-07-21 | 1981-07-21 | ベンズアルデヒド類の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5815935A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006045095A (ja) * | 2004-08-03 | 2006-02-16 | Central Glass Co Ltd | ３−ホルミル−５−トリフルオロメチルベンゾニトリル誘導体とその製造方法 |
-
1981
- 1981-07-21 JP JP56112977A patent/JPS5815935A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006045095A (ja) * | 2004-08-03 | 2006-02-16 | Central Glass Co Ltd | ３−ホルミル−５−トリフルオロメチルベンゾニトリル誘導体とその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS629576B2 (enrdf_load_stackoverflow) | 1987-02-28 |
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