SU322984A1 - Method of producing 1,10-decanedicarboxylic acid - Google Patents
Method of producing 1,10-decanedicarboxylic acid Download PDFInfo
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- SU322984A1 SU322984A1 SU701402379A SU1402379A SU322984A1 SU 322984 A1 SU322984 A1 SU 322984A1 SU 701402379 A SU701402379 A SU 701402379A SU 1402379 A SU1402379 A SU 1402379A SU 322984 A1 SU322984 A1 SU 322984A1
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- USSR - Soviet Union
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- ozonolysis
- producing
- acid
- decanedicarboxylic acid
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Изобретение относитс к способу получени дикарбоновых кислот, в частности 1,10-декандикарбоновой кислоты, котора может примен тьс в качестве пластификатора. Известен способ получени 1,10-декандикарбоновой кислоты озонолнзомt циклододецена, который провод т в растворе низших монокарбоновых кислот при с последуюlOHM окислительHfcBH разложением продуктов рэонолиза в токе кислорода или воздуха при посто нно повыиающе с температуре от 80 до . Осу ществление термоокислительного разложени продуктов озонолиза таким crtoco6oM приводит к Образованию побочных продуктов окислени перекисных продуктов озонолиза, что усложн ет процесс получени кислоты треб емого качества в св зи с необходимостью применени сложных и дорогосто п1их методов очистки. Выход целевого.продукта в извест ных способах не превышает 70% от теоретического. В предлагаемом способе получени 1,10-декандикарво«овой кислоты озонолиэом циклододецена идет в две ступени: перва - окисление продукт .ов озонолиза перекисью водорода в присутствии твер2№х кислотных катализаторов , например 1СУ-2/8, при температуре 50-70 С, втора - термиН ческое разложение (уже без кислорода и катализатора) продуктов окислени при температуре 90-110 С. Пос.пе охлаждени раствора отфильтровывают выпавшую 1,10-декандикарбоновую кислоту, отмывают водой от следов растворител и .высушивают. Выход кислоты составл ет не менее 98% от теоретического. Чистота продукта достигаетс 99,5%.. Пример 1. 1б,6г циклододецена (0,1 моль) раствор ют в 66,4 г 98%-ной уксусной кислоты. Через смесь со скоростью 100 л/ч и при пропускают .озонированный воздух (содержание озона Звес.%) до проскока озона. При этом образуетс 27,2 ,г (количественное превращение) продукта озонолиза циклододецена в растворе 54,4 г уксусной кислоты. 6 г уксусной кислоты уноситс токомThe invention relates to a process for the preparation of dicarboxylic acids, in particular 1,10-decanedicarboxylic acid, which can be used as a plasticizer. A known method for the preparation of 1,10-decanedicarboxylic acid by cyclododecene ozonolum, which is carried out in a solution of lower monocarboxylic acids with the oxidant HfcBH followed by lOHM decomposition of the rheonolysis products in a stream of oxygen or air at a constant temperature from 80 to. The realization of thermo-oxidative decomposition of ozonolysis products by such crtoco6oM leads to the formation of oxidation by-products of peroxide ozonolysis products, which complicates the process of obtaining acid of required quality due to the necessity of using complex purification methods. The yield of the target product in the known methods does not exceed 70% of the theoretical one. In the proposed method of producing 1,10-decanedicarvoic acid with ozonolium cyclododecene, there are two steps: first, oxidation of the product of ozonolysis with hydrogen peroxide in the presence of hydrated acid catalysts, for example, 1С – 2/8, at a temperature of 50–70 ° C, the second - thermal decomposition (already without oxygen and catalyst) of oxidation products at a temperature of 90-110 ° C. After cooling the solution, the precipitated 1,10-decanedicarboxylic acid is filtered off, washed with water from traces of the solvent and dried. The acid output is at least 98% of the theoretical. The purity of the product is 99.5%. Example 1. 1b, 6g cyclododecene (0.1 mol) is dissolved in 66.4 g of 98% acetic acid. Through the mixture at a rate of 100 l / h, and when air is passed. Ozonized air (ozone content Zves.%) To ozone leakage. This forms 27.2, g (quantitative conversion) of the product of cyclododecene ozonolysis in a solution of 54.4 g of acetic acid. 6 g of acetic acid is carried away
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU701402379A SU322984A1 (en) | 1970-02-17 | 1970-02-17 | Method of producing 1,10-decanedicarboxylic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU701402379A SU322984A1 (en) | 1970-02-17 | 1970-02-17 | Method of producing 1,10-decanedicarboxylic acid |
Publications (1)
Publication Number | Publication Date |
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SU322984A1 true SU322984A1 (en) | 1981-03-23 |
Family
ID=20449896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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SU701402379A SU322984A1 (en) | 1970-02-17 | 1970-02-17 | Method of producing 1,10-decanedicarboxylic acid |
Country Status (1)
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SU (1) | SU322984A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4606863A (en) * | 1983-06-02 | 1986-08-19 | New Japan Chemical Co., Ltd. | Process for preparing carboxylic acid |
-
1970
- 1970-02-17 SU SU701402379A patent/SU322984A1/en active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4606863A (en) * | 1983-06-02 | 1986-08-19 | New Japan Chemical Co., Ltd. | Process for preparing carboxylic acid |
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