JPH0519535B2 - - Google Patents
Info
- Publication number
- JPH0519535B2 JPH0519535B2 JP59107785A JP10778584A JPH0519535B2 JP H0519535 B2 JPH0519535 B2 JP H0519535B2 JP 59107785 A JP59107785 A JP 59107785A JP 10778584 A JP10778584 A JP 10778584A JP H0519535 B2 JPH0519535 B2 JP H0519535B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- boric acid
- oxycarboxylic
- carboxylic acid
- mixture
- 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 - Fee Related
Links
- 239000004327 boric acid Substances 0.000 claims description 49
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 30
- 239000002253 acid Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 23
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 238000005886 esterification reaction Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 11
- 239000001361 adipic acid Substances 0.000 claims description 8
- 235000011037 adipic acid Nutrition 0.000 claims description 8
- 150000001735 carboxylic acids Chemical class 0.000 claims description 8
- 239000003729 cation exchange resin Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000005691 triesters Chemical class 0.000 claims 1
- -1 borate ester Chemical class 0.000 description 15
- 239000000126 substance Substances 0.000 description 14
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 4
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000010446 mirabilite Substances 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 229940023913 cation exchange resins Drugs 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229940005605 valeric acid Drugs 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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59107785A JPS60252447A (ja) | 1984-05-28 | 1984-05-28 | エステル化物の製法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59107785A JPS60252447A (ja) | 1984-05-28 | 1984-05-28 | エステル化物の製法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60252447A JPS60252447A (ja) | 1985-12-13 |
| JPH0519535B2 true JPH0519535B2 (enrdf_load_stackoverflow) | 1993-03-17 |
Family
ID=14467958
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59107785A Granted JPS60252447A (ja) | 1984-05-28 | 1984-05-28 | エステル化物の製法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60252447A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109529869A (zh) * | 2018-12-05 | 2019-03-29 | 江苏师范大学 | 一种催化剂及其应用 |
-
1984
- 1984-05-28 JP JP59107785A patent/JPS60252447A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60252447A (ja) | 1985-12-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3841834B2 (ja) | マロン酸およびそのエステル | |
| US4172961A (en) | Production of 1,4-butanediol | |
| US4360406A (en) | Process for the preparation of tertiary butyl alcohol | |
| WO2001056970A1 (fr) | Procede de production de terephtalate de bis-?-hydroxyethyle de grande purete | |
| CN103429307A (zh) | 从稀水溶液中回收有机酸的方法 | |
| JPH0519535B2 (enrdf_load_stackoverflow) | ||
| CN101238090B (zh) | 制备l-(+)-乳酸的方法 | |
| JPH0840983A (ja) | 乳酸エステルの製造方法 | |
| US4360695A (en) | Continuous preparation of adiptic acid | |
| US5344975A (en) | Process for production of lower alkanoic acids | |
| EP0983993A1 (en) | Process for producing allyl-2-hydroxyisobutyrate | |
| JP4444443B2 (ja) | ポリエステル廃棄物からの有価成分回収方法 | |
| JP3174406B2 (ja) | エチルアルコールの製造方法 | |
| JP2002234883A (ja) | テトラヒドロフランの精製方法 | |
| US3867439A (en) | Preparation of potassium benzoate | |
| CA1195687A (en) | Process for producing polyols with at least one oxacyclopentane ring | |
| JPS6353167B2 (enrdf_load_stackoverflow) | ||
| US3957730A (en) | Recovery of pure 2-methyl-2-hydroxy-heptanone-6 | |
| JPH01165560A (ja) | アミノ酸のエステル化方法 | |
| JPH11335319A (ja) | α−ヒドロキシカルボン酸の製造方法 | |
| JP3205972B2 (ja) | ピラジン−２−カルボン酸エステルおよびその製造方法 | |
| CN114560752A (zh) | 一种2-甲基烯丙醇的合成方法 | |
| RU2063958C1 (ru) | Способ выделения кротонового альдегида | |
| JP2514001B2 (ja) | アセチンの製造方法 | |
| JP2866214B2 (ja) | アルカングリコールの製造法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |