JPS58172342A - アジポアルデヒド酸の製造方法 - Google Patents
アジポアルデヒド酸の製造方法Info
- Publication number
- JPS58172342A JPS58172342A JP57053908A JP5390882A JPS58172342A JP S58172342 A JPS58172342 A JP S58172342A JP 57053908 A JP57053908 A JP 57053908A JP 5390882 A JP5390882 A JP 5390882A JP S58172342 A JPS58172342 A JP S58172342A
- Authority
- JP
- Japan
- Prior art keywords
- cyclohexanone
- water
- ferric
- compound
- 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.)
- Granted
Links
- 239000002253 acid Substances 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-UHFFFAOYSA-N 0.000 title abstract description 8
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 150000002504 iridium compounds Chemical class 0.000 claims abstract description 6
- 229910052742 iron Inorganic materials 0.000 claims abstract description 6
- 230000001590 oxidative effect Effects 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 20
- 239000003054 catalyst Substances 0.000 abstract description 9
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract description 7
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract description 7
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 abstract description 4
- 150000002506 iron compounds Chemical class 0.000 abstract description 3
- 229910021639 Iridium tetrachloride Inorganic materials 0.000 abstract description 2
- 229960002089 ferrous chloride Drugs 0.000 abstract description 2
- 235000003891 ferrous sulphate Nutrition 0.000 abstract description 2
- 239000011790 ferrous sulphate Substances 0.000 abstract description 2
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 abstract description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 abstract description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- CALMYRPSSNRCFD-UHFFFAOYSA-J tetrachloroiridium Chemical compound Cl[Ir](Cl)(Cl)Cl CALMYRPSSNRCFD-UHFFFAOYSA-J 0.000 abstract description 2
- FEONEKOZSGPOFN-UHFFFAOYSA-K tribromoiron Chemical compound Br[Fe](Br)Br FEONEKOZSGPOFN-UHFFFAOYSA-K 0.000 abstract description 2
- 239000000543 intermediate Substances 0.000 abstract 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 abstract 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 238000007254 oxidation reaction Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 5
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- PNPPVRALIYXJBW-UHFFFAOYSA-N 6-oxohexanoic acid Chemical compound OC(=O)CCCCC=O PNPPVRALIYXJBW-UHFFFAOYSA-N 0.000 description 1
- 241000272201 Columbiformes Species 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 235000021167 banquet Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- -1 iron Chemical class 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- ACKFDYCQCBEDNU-UHFFFAOYSA-J lead(2+);tetraacetate Chemical compound [Pb+2].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O ACKFDYCQCBEDNU-UHFFFAOYSA-J 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000003756 stirring 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
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57053908A JPS58172342A (ja) | 1982-04-02 | 1982-04-02 | アジポアルデヒド酸の製造方法 |
US06/475,646 US4649217A (en) | 1982-04-02 | 1983-03-15 | Process for producing oxocarboxylic acids |
DE8383103186T DE3360258D1 (en) | 1982-04-02 | 1983-03-30 | A process for producing oxocarboxylic acids |
EP83103186A EP0091091B1 (en) | 1982-04-02 | 1983-03-30 | A process for producing oxocarboxylic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57053908A JPS58172342A (ja) | 1982-04-02 | 1982-04-02 | アジポアルデヒド酸の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58172342A true JPS58172342A (ja) | 1983-10-11 |
JPH042583B2 JPH042583B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-01-20 |
Family
ID=12955810
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57053908A Granted JPS58172342A (ja) | 1982-04-02 | 1982-04-02 | アジポアルデヒド酸の製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58172342A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
1982
- 1982-04-02 JP JP57053908A patent/JPS58172342A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH042583B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-01-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Almeida et al. | Ruthenium (II)‐Catalyzed Oppenauer‐Type Oxidation of Secondary Alcohols | |
JPH08127550A (ja) | 金−酸化チタン含有触媒による炭化水素の部分酸化方法 | |
JPH01146837A (ja) | シクロヘキセノンの脱水素方法 | |
RU2210562C2 (ru) | Способ окисления углеводородов | |
ATE294134T1 (de) | Direktsynthese von wasserstoffperoxid in einem mehrkomponenten-lösungsmittelsystem | |
US3444189A (en) | Vinyl acetate synthesis | |
US6274764B1 (en) | Process for one step gas phase production of acetic acid from ethylene | |
Chou et al. | Effect of interface mass transfer on the liquid-phase oxidation of acetaldehyde | |
US4393144A (en) | Method for producing methanol | |
US3804902A (en) | Process for producing acetone | |
JPS58172342A (ja) | アジポアルデヒド酸の製造方法 | |
Kamiya et al. | Catalysis of manganese salts in the autoxidation of cyclohexanone | |
JPH07116097B2 (ja) | ピロメリツト酸の製造方法 | |
KR0156272B1 (ko) | 전환반응용 촉매 및 이의 제조방법, 그리고 이를 이용한 에틸렌의 제조방법 | |
US3231620A (en) | Production of carbonyl compounds | |
US4115440A (en) | Selenium catalyzed decomposition of peroxide intermediates resulting from the autoxidation of acrolein and methacrolein | |
JPH10231266A (ja) | 2−メチル−1,4−ベンゾキノンの製造方法 | |
JPS6345666B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US6075170A (en) | Process for preparing cyclohexanol and cyclohexanone | |
SU1727877A1 (ru) | Катализатор дл жидкофазного окислени ацетальдегида | |
JPH01117859A (ja) | 芳香族過カルボン酸の製造法 | |
Tagawa et al. | Liquid phase oxidation of benzene to phenol over K2Cr2O7/SiO2 | |
JP3747239B2 (ja) | プロピレンオキシドの製造方法 | |
SU997797A1 (ru) | Катализатор дл окислени ацетальдегида | |
SU1097371A1 (ru) | Катализатор дл жидкофазного окислени ацетальдегида |