JPH0461862B2 - - Google Patents
Info
- Publication number
- JPH0461862B2 JPH0461862B2 JP59104462A JP10446284A JPH0461862B2 JP H0461862 B2 JPH0461862 B2 JP H0461862B2 JP 59104462 A JP59104462 A JP 59104462A JP 10446284 A JP10446284 A JP 10446284A JP H0461862 B2 JPH0461862 B2 JP H0461862B2
- Authority
- JP
- Japan
- Prior art keywords
- chloride
- reaction
- benzal
- catalyst
- xylene
- 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
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 10
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 claims description 9
- 239000011667 zinc carbonate Substances 0.000 claims description 9
- 235000004416 zinc carbonate Nutrition 0.000 claims description 9
- 229910000010 zinc carbonate Inorganic materials 0.000 claims description 9
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 8
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 claims description 8
- 229940007718 zinc hydroxide Drugs 0.000 claims description 8
- 229910021511 zinc hydroxide Inorganic materials 0.000 claims description 8
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 19
- -1 benzal halides Chemical class 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical class ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 6
- 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 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 150000003935 benzaldehydes Chemical class 0.000 description 3
- 229960003280 cupric chloride Drugs 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- DMIYKWPEFRFTPY-UHFFFAOYSA-N 2,6-dichlorobenzaldehyde Chemical compound ClC1=CC=CC(Cl)=C1C=O DMIYKWPEFRFTPY-UHFFFAOYSA-N 0.000 description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 2
- 229940045803 cuprous chloride Drugs 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- UFJYKWQUTDGGPV-UHFFFAOYSA-N 1,2-bis(dichloromethyl)benzene Chemical group ClC(Cl)C1=CC=CC=C1C(Cl)Cl UFJYKWQUTDGGPV-UHFFFAOYSA-N 0.000 description 1
- HBTZFDIPZCSOJI-UHFFFAOYSA-N 1,3,5-trichloro-2-(dichloromethyl)benzene Chemical compound ClC(Cl)C1=C(Cl)C=C(Cl)C=C1Cl HBTZFDIPZCSOJI-UHFFFAOYSA-N 0.000 description 1
- ZMCUKNMLHBAGMS-UHFFFAOYSA-N 1,3-bis(dibromomethyl)benzene Chemical group BrC(Br)C1=CC=CC(C(Br)Br)=C1 ZMCUKNMLHBAGMS-UHFFFAOYSA-N 0.000 description 1
- VIQBABDKNOOCQD-UHFFFAOYSA-N 1,4-bis(dibromomethyl)benzene Chemical group BrC(Br)C1=CC=C(C(Br)Br)C=C1 VIQBABDKNOOCQD-UHFFFAOYSA-N 0.000 description 1
- DSYDSGAYKSQVOV-UHFFFAOYSA-N 1-(dibromomethyl)-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(C(Br)Br)C=C1 DSYDSGAYKSQVOV-UHFFFAOYSA-N 0.000 description 1
- RTDHYMHZYQCBDN-UHFFFAOYSA-N 1-(dibromomethyl)-4-ethylbenzene Chemical compound CCC1=CC=C(C(Br)Br)C=C1 RTDHYMHZYQCBDN-UHFFFAOYSA-N 0.000 description 1
- ZQNQSIPAAGRZAU-UHFFFAOYSA-N 1-(dibromomethyl)-4-fluorobenzene Chemical compound FC1=CC=C(C(Br)Br)C=C1 ZQNQSIPAAGRZAU-UHFFFAOYSA-N 0.000 description 1
- LRQSJOUIUVTBAJ-UHFFFAOYSA-N 1-(dibromomethyl)-4-methoxybenzene Chemical compound COC1=CC=C(C(Br)Br)C=C1 LRQSJOUIUVTBAJ-UHFFFAOYSA-N 0.000 description 1
- HQHJZSCJOXQOAY-UHFFFAOYSA-N 1-(dibromomethyl)-4-methylbenzene Chemical compound CC1=CC=C(C(Br)Br)C=C1 HQHJZSCJOXQOAY-UHFFFAOYSA-N 0.000 description 1
- MKHFRSNFHCJQIQ-UHFFFAOYSA-N 1-(dibromomethyl)-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(C(Br)Br)C=C1 MKHFRSNFHCJQIQ-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
- QLYKBXXWYGHMRB-UHFFFAOYSA-N 1-(dichloromethyl)-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(C(Cl)Cl)=C1 QLYKBXXWYGHMRB-UHFFFAOYSA-N 0.000 description 1
- GDZMMXXMEMTSJY-UHFFFAOYSA-N 1-(dichloromethyl)-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(C(Cl)Cl)C=C1 GDZMMXXMEMTSJY-UHFFFAOYSA-N 0.000 description 1
- PWKUMFYUILTTMD-UHFFFAOYSA-N 1-(dichloromethyl)-4-ethylbenzene Chemical compound CCC1=CC=C(C(Cl)Cl)C=C1 PWKUMFYUILTTMD-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
- UKVWNSDFMYZNKC-UHFFFAOYSA-N 1-(dichloromethyl)-4-methoxybenzene Chemical compound COC1=CC=C(C(Cl)Cl)C=C1 UKVWNSDFMYZNKC-UHFFFAOYSA-N 0.000 description 1
- RGDYIHSZBVIIND-UHFFFAOYSA-N 1-(dichloromethyl)-4-methylbenzene Chemical compound CC1=CC=C(C(Cl)Cl)C=C1 RGDYIHSZBVIIND-UHFFFAOYSA-N 0.000 description 1
- KWWRZTBCOVYCIU-UHFFFAOYSA-N 1-(dichloromethyl)-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(C(Cl)Cl)C=C1 KWWRZTBCOVYCIU-UHFFFAOYSA-N 0.000 description 1
- GAUQRPKIMSLERN-UHFFFAOYSA-N 1-(dichloromethyl)-4-phenoxybenzene Chemical compound C1=CC(C(Cl)Cl)=CC=C1OC1=CC=CC=C1 GAUQRPKIMSLERN-UHFFFAOYSA-N 0.000 description 1
- SXTBVNDWRMMWFE-UHFFFAOYSA-N 1-(dichloromethyl)-4-propylbenzene Chemical compound CCCC1=CC=C(C(Cl)Cl)C=C1 SXTBVNDWRMMWFE-UHFFFAOYSA-N 0.000 description 1
- PGLAXDZKOAPBHY-UHFFFAOYSA-N 1-bromo-4-(dibromomethyl)benzene Chemical compound BrC(Br)C1=CC=C(Br)C=C1 PGLAXDZKOAPBHY-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
- JHUHEBLQVJNTOC-UHFFFAOYSA-N 1-chloro-4-(dibromomethyl)benzene Chemical compound ClC1=CC=C(C(Br)Br)C=C1 JHUHEBLQVJNTOC-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
- FEWDXGMBVQULLN-UHFFFAOYSA-N 1-hydroxy-2-phenyl-1,5,6,7-tetrahydro-4H-benzimidazol-4-one Chemical compound ON1C=2CCCC(=O)C=2N=C1C1=CC=CC=C1 FEWDXGMBVQULLN-UHFFFAOYSA-N 0.000 description 1
- OUOHINWZCBGQDY-UHFFFAOYSA-N 1-tert-butyl-4-(dibromomethyl)benzene Chemical compound CC(C)(C)C1=CC=C(C(Br)Br)C=C1 OUOHINWZCBGQDY-UHFFFAOYSA-N 0.000 description 1
- HDTAUMIOSWQZRW-UHFFFAOYSA-N 2,2-dichloro-2-phenylacetonitrile Chemical compound N#CC(Cl)(Cl)C1=CC=CC=C1 HDTAUMIOSWQZRW-UHFFFAOYSA-N 0.000 description 1
- GYQNIXGSKFFVIK-UHFFFAOYSA-N 4-(dibromomethyl)benzonitrile Chemical compound BrC(Br)C1=CC=C(C#N)C=C1 GYQNIXGSKFFVIK-UHFFFAOYSA-N 0.000 description 1
- HGFVOZQVKMBMQH-UHFFFAOYSA-N O(C1=CC=CC=C1)C1=CC=C(C(Br)Br)C=C1 Chemical compound O(C1=CC=CC=C1)C1=CC=C(C(Br)Br)C=C1 HGFVOZQVKMBMQH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000005406 washing Methods 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 |
|---|---|---|---|
| JP59104462A JPS60248640A (ja) | 1984-05-25 | 1984-05-25 | ベンズアルデヒド類の製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59104462A JPS60248640A (ja) | 1984-05-25 | 1984-05-25 | ベンズアルデヒド類の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60248640A JPS60248640A (ja) | 1985-12-09 |
| JPH0461862B2 true JPH0461862B2 (enrdf_load_stackoverflow) | 1992-10-02 |
Family
ID=14381252
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59104462A Granted JPS60248640A (ja) | 1984-05-25 | 1984-05-25 | ベンズアルデヒド類の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60248640A (enrdf_load_stackoverflow) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW228517B (enrdf_load_stackoverflow) * | 1992-11-26 | 1994-08-21 | Hoechst Ag | |
| TW290534B (enrdf_load_stackoverflow) * | 1992-11-26 | 1996-11-11 | Hoechst Ag | |
| CN104447250A (zh) * | 2014-12-24 | 2015-03-25 | 常熟市新华化工有限公司 | 一种由对氯甲苯合成对氯苯甲醛的方法 |
-
1984
- 1984-05-25 JP JP59104462A patent/JPS60248640A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60248640A (ja) | 1985-12-09 |