DE277392C - - Google Patents
Info
- Publication number
- DE277392C DE277392C DENDAT277392D DE277392DA DE277392C DE 277392 C DE277392 C DE 277392C DE NDAT277392 D DENDAT277392 D DE NDAT277392D DE 277392D A DE277392D A DE 277392DA DE 277392 C DE277392 C DE 277392C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- reduced
- disecondary
- glycols
- aliphatic aldehydes
- 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.)
- Active
Links
- 150000002334 glycols Chemical group 0.000 claims description 5
- -1 saturated aliphatic aldehydes Chemical class 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical class [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/29—Coupling reactions
- C25B3/295—Coupling reactions hydrodimerisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE277392C true DE277392C (enrdf_load_stackoverflow) |
Family
ID=533492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT277392D Active DE277392C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE277392C (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2457911A1 (fr) * | 1979-06-01 | 1980-12-26 | Toyo Soda Mfg Co Ltd | Procede de production de glycol a partir de formaldehyde par electrolyse |
EP0024178A3 (en) * | 1979-08-14 | 1981-05-20 | E.I. Du Pont De Nemours And Company | Process for preparing alkanediols by electrochemical coupling of halohydrins, alkanediols, when produced by such process, and an electrolytic cell suitable for carrying out the process |
-
0
- DE DENDAT277392D patent/DE277392C/de active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2457911A1 (fr) * | 1979-06-01 | 1980-12-26 | Toyo Soda Mfg Co Ltd | Procede de production de glycol a partir de formaldehyde par electrolyse |
EP0024178A3 (en) * | 1979-08-14 | 1981-05-20 | E.I. Du Pont De Nemours And Company | Process for preparing alkanediols by electrochemical coupling of halohydrins, alkanediols, when produced by such process, and an electrolytic cell suitable for carrying out the process |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0011712B1 (de) | Verfahren zur Herstellung von in 4-Stellung substituierten Benzaldehyddialkylacetalen | |
EP0012240B1 (de) | Verfahren zur Herstellung von gegebenenfalls substituierten Benzaldehyd-dialkylacetalen | |
DE277392C (enrdf_load_stackoverflow) | ||
EP0275489B1 (de) | Neue Benzaldehydderivate, ihre Herstellung und Verwendung | |
DE2008675A1 (de) | Verfahren zur Herstellung von tertiären Acetylenglykolen durch Umsetzung von Acetylen mit Ketonen | |
DE2547383A1 (de) | Verfahren zur herstellung von p-benzochinondiketalen | |
EP0054698B1 (de) | 4,4'-Diphenylether-dialdehyd-bis-dimethylacetal und ein Verfahren zu seiner Herstellung | |
DE233519C (enrdf_load_stackoverflow) | ||
EP0001211A1 (de) | Verfahren zur Entfernung von Bleiionen aus Formose und Verwendung der so erhaltenen Formose zur Herstellung von Kunststoff und metholierter Formosen | |
DE10043789A1 (de) | Verfahren zur Herstellung von Orthocarbonsäuretrialkylestern | |
DE2623089A1 (de) | Verfahren zur herstellung von perfluor-4-oxo-2,5-dimethyl-2-fluorcarbonyl-1,3-dioxolan | |
EP0053261B1 (de) | Verfahren zur Herstellung eines Gemisches von Ketalen des Trimethyl-p-benzochinons | |
DE2360494A1 (de) | Verfahren zur herstellung von alkylsubstituierten hydrochinonen | |
EP0393668B1 (de) | Verfahren zur Herstellung von Benzaldehyddialkylacetalen und neue Benzaldehyddialkylacetale | |
DE254713C (enrdf_load_stackoverflow) | ||
DE160103C (enrdf_load_stackoverflow) | ||
Swann et al. | The Electrolytic Reduction of Diisopropyl Ketone in Acid Solution | |
DE274201C (enrdf_load_stackoverflow) | ||
DE266520C (enrdf_load_stackoverflow) | ||
DE2432218A1 (de) | Verfahren zur herstellung von 1-methyladamantan | |
DE1944279A1 (de) | Verfahren zur Herstellung von Octadienen und Decatrienen | |
EP0339521B1 (de) | Verfahren zur Herstellung von Tetralinderivaten und neue Tetralinderivate | |
DE575350C (de) | Verfahren zur Herstellung von Acetbutyraldol | |
AT69318B (de) | Verfahren zur Darstellung von 1.3-Butylenglykol. | |
DE1944277A1 (de) | Verfahren zur Herstellung von Butan-Derivaten |