DE292066C - - Google Patents
Info
- Publication number
- DE292066C DE292066C DENDAT292066D DE292066DA DE292066C DE 292066 C DE292066 C DE 292066C DE NDAT292066 D DENDAT292066 D DE NDAT292066D DE 292066D A DE292066D A DE 292066DA DE 292066 C DE292066 C DE 292066C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- acid
- substitution products
- methyl
- alkyl
- 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
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 10
- 238000006467 substitution reaction Methods 0.000 claims description 7
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 5
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 5
- 150000007513 acids Chemical group 0.000 claims description 3
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 3
- 150000004056 anthraquinones Chemical class 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 239000002253 acid Substances 0.000 description 9
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 8
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/34—Quinones containing groups having oxygen atoms singly bound to carbon atoms the quinoid structure being part of a condensed ring system having three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE292066C true DE292066C (enrdf_load_stackoverflow) |
Family
ID=546882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT292066D Active DE292066C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE292066C (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3419966B1 (en) * | 2016-02-22 | 2020-03-25 | Alcon Inc. | Uv-absorbing vinylic monomers and uses thereof |
-
0
- DE DENDAT292066D patent/DE292066C/de active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3419966B1 (en) * | 2016-02-22 | 2020-03-25 | Alcon Inc. | Uv-absorbing vinylic monomers and uses thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE261689C (enrdf_load_stackoverflow) | ||
| DE2003461A1 (de) | Verfahren zur Herstellung von 2-Alkylpyridaziniumverbindungen | |
| DE2437882C3 (de) | Verfahren zur Herstellung von Estern des 3-Phenoxybenzylalkohols | |
| DE292066C (enrdf_load_stackoverflow) | ||
| DE1795500A1 (de) | Verfahren zur Herstellung von Benzodiazepin-Derivaten | |
| DE1804693A1 (de) | Chemisches Verfahren | |
| CH635088A5 (de) | Verfahren zur herstellung von quartaeren sulfoalkylsalzen. | |
| DE2065365A1 (de) | 1,3-disubstituierte azetidine und verfahren zu deren herstellung | |
| DE2416594C2 (de) | Verfahren zur Herstellung vn 2, 2',3,3'-Tetracarbonsäurediphenylätherdianhydrid | |
| DE278778C (enrdf_load_stackoverflow) | ||
| DE871449C (de) | Verfahren zur Herstellung des Pentaerythrit-dichlorhydrin-monoschwefligsaeureesters | |
| DE2033644C3 (de) | Verfahren zur Herstellung von 5,6, 7,7a-Tetrahydro-1 ß -hydroxy-5-oxo-4-indancarbonsäuren bzw. deren Aethern und Estern | |
| DE591937C (de) | Verfahren zur Darstellung von Arsenverbindungen der Chinolinreihe | |
| DE280971C (enrdf_load_stackoverflow) | ||
| DE522060C (de) | Verfahren zur Darstellung von Chlorderivaten des Pyridins | |
| DE581328C (de) | Verfahren zur Darstellung von Acridon und substituierten Acridonen | |
| DE557665C (de) | Verfahren zur Darstellung von stickstoffhaltigen Abkoemmlingen aromatischer Verbindungen | |
| DE1931870C3 (de) | Verfahren zur Herstellung von 5-Phenyl-t3-dihydro-2H-l,4-benzodiazepin-2-on-derivaten | |
| DE152548C (enrdf_load_stackoverflow) | ||
| DE2660213C2 (de) | Verfahren zur Herstellung von Acylcyaniden | |
| DE67115C (de) | Verfahren und Darstellung von o-Tolylrosindulin | |
| DE1695893C (de) | Verfahren zur Herstellung von 4 Amino 5 acylamidomethyl pynmidinen | |
| DE81245C (enrdf_load_stackoverflow) | ||
| DE2223128C3 (de) | Verfahren zur Herstellung von Derivaten der Hexahydrophthalsäure | |
| DE603101C (de) | Verfahren zur Herstellung von Kondensationsprodukten |