DE175585C - - Google Patents
Info
- Publication number
- DE175585C DE175585C DENDAT175585D DE175585DA DE175585C DE 175585 C DE175585 C DE 175585C DE NDAT175585 D DENDAT175585 D DE NDAT175585D DE 175585D A DE175585D A DE 175585DA DE 175585 C DE175585 C DE 175585C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- acids
- bromine
- dialkylmalonic
- converted
- 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
- 239000002253 acid Substances 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
- CBRCMTPPRWRXJS-UHFFFAOYSA-N 2-bromo-2-ethylbutanoic acid Chemical compound CCC(Br)(CC)C(O)=O CBRCMTPPRWRXJS-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 125000000218 acetic acid group Chemical class C(C)(=O)* 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- LTMRRSWNXVJMBA-UHFFFAOYSA-N 2,2-diethylpropanedioic acid Chemical compound CCC(CC)(C(O)=O)C(O)=O LTMRRSWNXVJMBA-UHFFFAOYSA-N 0.000 description 1
- VKEWQHFBEKFBLA-UHFFFAOYSA-N 2-bromo-2-propylpentanoic acid Chemical compound CCCC(Br)(C(O)=O)CCC VKEWQHFBEKFBLA-UHFFFAOYSA-N 0.000 description 1
- IUWKUVZFZLNCRH-UHFFFAOYSA-N BrCCC(C(=O)O)CCC Chemical compound BrCCC(C(=O)O)CCC IUWKUVZFZLNCRH-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- NIJJYAXOARWZEE-UHFFFAOYSA-N Valproic acid Chemical compound CCCC(C(O)=O)CCC NIJJYAXOARWZEE-UHFFFAOYSA-N 0.000 description 1
- 150000003869 acetamides Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N malonic acid group Chemical group C(CC(=O)O)(=O)O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE175585C true DE175585C (enExample) |
Family
ID=440213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT175585D Active DE175585C (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE175585C (enExample) |
-
0
- DE DENDAT175585D patent/DE175585C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1941536A1 (de) | 1-Alkyl-2-aminomethylpyrrolidine sowie Verfahren zur Herstellung dieser Verbindungen und deren Zwischenprodukte | |
| DE69220516T2 (de) | Verfahren zur Produktion und Reinigung von aliphatischen Aminen | |
| DE1263743B (de) | Verfahren zur Herstellung von substituierten Acetamiden | |
| AT203485B (de) | Verfahren zur Herstellung von neuen Dinitrophenylmethacrylaten | |
| DE570677C (de) | Verfahren zur Herstellung von Oxyalkylaminoverbindungen | |
| DE681850C (de) | Verfahren zur Herstellung quaternaerer Stickstoffverbindungen | |
| DE4128351A1 (de) | Verfahren zur herstellung von nitrobenzoesaeuren und anthranilsaeuren | |
| DE2732409A1 (de) | Verfahren zur herstellung von diaminoalkoxybenzolen | |
| DE97101C (enExample) | ||
| DE205849C (enExample) | ||
| DE944623C (de) | Zusatzmittel fuer technische OEle und Fette auf Minerlaoelbasis | |
| DE870252C (de) | Verfahren zur Darstellung von ª†-Oxocarbonsaeuren | |
| DE173610C (enExample) | ||
| DE120465C (enExample) | ||
| AT83028B (de) | Verfahren zur Darstellung hydrierter Naphtaline. | |
| DE949654C (de) | Verfahren zur Herstellung von Acrylsaeure und ihren funktionellen Derivaten | |
| DE189841C (enExample) | ||
| DE625324C (de) | Verfahren zur Reinigung von synthetischem Methanol | |
| DE1910463A1 (de) | Verfahren zur Herstellung von Carbonsaeureanhydriden | |
| DE917425C (de) | Verfahren zur Herstellung von Azomethinen | |
| DE157840C (enExample) | ||
| DE2414002A1 (de) | Reinigung von n,n'-disubstituierten p-phenylendiamin-antiozonisierungsmitteln und oelstabilisatoren | |
| DE843414C (de) | Verfahren zur Herstellung von 2-Aryl-3,4,6-triketo-2,3,4,5,6,7-hexahydro-pyrazolpyridinen | |
| DE946141C (de) | Verfahren zur Herstellung von Hexahydrophthalimiden, die am Stickstoffatom durch Kohlenwasserstoffreste substituiert sind | |
| AT164031B (de) | Verfahren zur Herstellung von 2,4,6-Triaminophenyl-mono-äthern |