DE143197C - - Google Patents
Info
- Publication number
- DE143197C DE143197C DENDAT143197D DE143197DA DE143197C DE 143197 C DE143197 C DE 143197C DE NDAT143197 D DENDAT143197 D DE NDAT143197D DE 143197D A DE143197D A DE 143197DA DE 143197 C DE143197 C DE 143197C
- Authority
- DE
- Germany
- Prior art keywords
- sulfuric acid
- solution
- condensation products
- reduction
- ammonia
- 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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 31
- 239000007859 condensation product Substances 0.000 claims description 11
- 150000001412 amines Chemical class 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000003934 aromatic aldehydes Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000002192 fatty aldehydes Chemical class 0.000 claims 1
- 239000000243 solution Substances 0.000 description 12
- 150000001299 aldehydes Chemical class 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 238000005868 electrolysis reaction Methods 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- HUMNYLRZRPPJDN-UHFFFAOYSA-N Benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 229910052570 clay Inorganic materials 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N Hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000001476 alcoholic Effects 0.000 description 3
- 150000004677 hydrates Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VUYRFIIFTJICNA-LKNRODPVSA-N (E)-N-[[(E)-benzylideneamino]-phenylmethyl]-1-phenylmethanimine Chemical compound C=1C=CC=CC=1/C=N/C(C=1C=CC=CC=1)\N=C\C1=CC=CC=C1 VUYRFIIFTJICNA-LKNRODPVSA-N 0.000 description 2
- 229960000583 Acetic Acid Drugs 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N Benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- RIWRFSMVIUAEBX-UHFFFAOYSA-N N-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 229940095076 benzaldehyde Drugs 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-Trioxane Chemical group C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- VASMRQAVWVVDPA-UHFFFAOYSA-N 1,3,5-triphenyl-1,3,5-triazinane Chemical compound C1N(C=2C=CC=CC=2)CN(C=2C=CC=CC=2)CN1C1=CC=CC=C1 VASMRQAVWVVDPA-UHFFFAOYSA-N 0.000 description 1
- RNCAEEKHAQHORD-UHFFFAOYSA-N C=C.C(C1=CC=CC=C1)N Chemical compound C=C.C(C1=CC=CC=C1)N RNCAEEKHAQHORD-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N Diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- LIWAQLJGPBVORC-UHFFFAOYSA-N Ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 1
- 241001072332 Monia Species 0.000 description 1
- UVEWQKMPXAHFST-UHFFFAOYSA-N N,1-diphenylmethanimine Chemical compound C=1C=CC=CC=1C=NC1=CC=CC=C1 UVEWQKMPXAHFST-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-Methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- GTWJETSWSUWSEJ-UHFFFAOYSA-N N-benzylaniline Chemical compound C=1C=CC=CC=1CNC1=CC=CC=C1 GTWJETSWSUWSEJ-UHFFFAOYSA-N 0.000 description 1
- IIVYBNBDIDWPQV-UHFFFAOYSA-N N-ethyl-1-phenylmethanimine Chemical compound CCN=CC1=CC=CC=C1 IIVYBNBDIDWPQV-UHFFFAOYSA-N 0.000 description 1
- HXTGGPKOEKKUQO-UHFFFAOYSA-N N-methyl-1-phenylmethanimine Chemical compound CN=CC1=CC=CC=C1 HXTGGPKOEKKUQO-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N ethyl amine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- -1 ethylidene imine Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011133 lead Substances 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001023 sodium amalgam Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE143197C true DE143197C (zh) |
Family
ID=410704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT143197D Active DE143197C (zh) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE143197C (zh) |
-
0
- DE DENDAT143197D patent/DE143197C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0012215B1 (de) | 2-Hydroxybutansulfonsaures Cholin und dessen Verwendung als Leitsalz | |
DE2404560C3 (de) | Verfahren zur Herstellung von Sebacinsäure | |
DE1226567B (de) | Verfahren zur Herstellung von trans-Hexahydroterephthalsaeure | |
DE143197C (zh) | ||
DE108838C (zh) | ||
DE2403446C2 (de) | Verfahren zur Herstellung hydrierter Indole | |
DE2248562A1 (de) | Verfahren zur herstellung von dicarbonsaeurediestern durch elektrochemische kondensation von dicarbonsaeuremonoestern | |
DE284533C (zh) | ||
DE3028757A1 (de) | Verfahren zur herstellung von p-tert.-butylbenzaldehyd | |
DE177490C (zh) | ||
DE254861C (zh) | ||
DE1793568B1 (de) | Verfahren zur Herstellung von paraffinischen Dicarbonsaeure- oder Teracarbonsaeureamiden | |
DE964773C (de) | Verfahren zur Herstellung von Cycloalkylhydroxylaminen | |
DE247454C (zh) | ||
DE169730C (zh) | ||
DE2058237C (zh) | ||
DE966201C (de) | Verfahren zur Herstellung von Cyclohexanonoxim durch katalytische Hydrierung von Nitrocyclohexansalzen | |
DE2111606B2 (de) | Verfahren zur Herstellung eines Diastereoisomerengemisches von Zearalanol | |
DE148054C (zh) | ||
DE116942C (zh) | ||
DE2237612A1 (de) | Verfahren zur herstellung von benzylalkohol | |
DE324920C (de) | Verfahren zur Darstellung von Pinakon | |
DE2854487A1 (de) | Verfahren zur herstellung von oxalsaeure aus kohlendioxid und vorrichtung zu dessen durchfuehrung | |
DE1443445A1 (de) | Verfahren zur Herstellung von mono- und difunktionellen Fluoralkanderivaten | |
DE1130821B (de) | Verfahren zur Herstellung unsymmetrischer Dialkylhydrazine |