SU415038A1 - - Google Patents
Info
- Publication number
- SU415038A1 SU415038A1 SU1759891A SU1759891A SU415038A1 SU 415038 A1 SU415038 A1 SU 415038A1 SU 1759891 A SU1759891 A SU 1759891A SU 1759891 A SU1759891 A SU 1759891A SU 415038 A1 SU415038 A1 SU 415038A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- catalyst
- acids
- mixture
- yield
- Prior art date
Links
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 description 6
- 239000001361 adipic acid Substances 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- 229910001882 dioxygen Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000000703 Cerium Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical class [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- -1 fatty acid salts Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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 |
---|---|---|---|
SU1759891A SU415038A1 (enrdf_load_stackoverflow) | 1972-03-16 | 1972-03-16 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1759891A SU415038A1 (enrdf_load_stackoverflow) | 1972-03-16 | 1972-03-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU415038A1 true SU415038A1 (enrdf_load_stackoverflow) | 1974-02-15 |
Family
ID=20506720
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1759891A SU415038A1 (enrdf_load_stackoverflow) | 1972-03-16 | 1972-03-16 |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU415038A1 (enrdf_load_stackoverflow) |
-
1972
- 1972-03-16 SU SU1759891A patent/SU415038A1/ru active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Mehltretter et al. | Sugar oxidation, saccharic and oxalic acids by the nitric acid oxidation of dextrose | |
US3856833A (en) | Method for the production of aldehydic acids | |
CN103209951A (zh) | 酮基羧酸、酮基羧酸酯、其制造和使用方法 | |
US2515304A (en) | Hydrolysis of 2,5-dihydrofurans to produce unsaturated dicarbonyl compounds | |
SU415038A1 (enrdf_load_stackoverflow) | ||
Collie et al. | LXXII.—An isomeric change of dehydracetic acid | |
US3076034A (en) | Preparation of tertiary phosphine oxides | |
US4550180A (en) | Method for manufacture of N-formylaspartic anhydride | |
US2862940A (en) | Process for the production of omegaamino acids | |
JPS6024781B2 (ja) | シス−2−ヒドロキシ−2−フエニル−r−1−シクロヘキサンカルボン酸の製造法 | |
JPS6023345A (ja) | グリオキシル酸エステルの製法 | |
US3123632A (en) | Process for the production of the | |
JPS5814434B2 (ja) | τ−ピロン製造のための中間体 | |
US2820820A (en) | Method for oxidizing glutaraldehydes | |
US2165184A (en) | Process for producing ascorbic acid | |
US3197488A (en) | Synthesis of keto-carboxylic acids and ketones | |
HU203080B (en) | Process for producing azetidine-3-carboxylic acid derivatives and their alkali metal, calcium, magnesium or barium salts | |
RU982317C (ru) | Способ получени алифатических дикарбоновых кислот | |
JP2938225B2 (ja) | アリルアルコールの製法 | |
US2967874A (en) | Process for increasing the chain length of levulinic acid | |
SU825494A1 (ru) | СПОСОБ .ПОЛУЧЕНИЯ ХЛОРЛНГИДРИДА2 , :'-ДИМЕТИЛ-2-АЦЕТИЛОКСИУКСУСНОЙ КИСЛОТЫ1Изобретение относитс к органической химии, конкретно к усовершенствованному способу получени хлоран- гидрида 2,2-диметил-2-ацетилоксиук- сусной кислоты формулы.^»^-c-cta^^"^ 1)-С-СНзо(1)который используетс в р де препаративных синтезов дл получени продуктов взаимодействи гидроперекиси трет-бутила с ацилированными производными хлорангидридов с1-оксикарбо- новых кислот.Наиболее близким по технической сущности к предлагаемому вл етсй способ получени адилированных производных хлорангидридов с6~оксикарбо- новых кислот, в частности соединени | |
JP4022677B2 (ja) | ピロガロールの製造方法 | |
SU405863A1 (enrdf_load_stackoverflow) | ||
SU426361A3 (ru) | СПОСОБ ПОЛУЧЕНИЯ ( + )-р-АМИНО- р- | |
SU905225A1 (ru) | Способ получени ди-или полиоксисоединений |