DE272690C - - Google Patents
Info
- Publication number
- DE272690C DE272690C DENDAT272690D DE272690DA DE272690C DE 272690 C DE272690 C DE 272690C DE NDAT272690 D DENDAT272690 D DE NDAT272690D DE 272690D A DE272690D A DE 272690DA DE 272690 C DE272690 C DE 272690C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- resorcinol
- arsenic acid
- arsenic
- heated
- 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.)
- Expired
Links
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 17
- DJHGAFSJWGLOIV-UHFFFAOYSA-N Arsenic acid Chemical compound O[As](O)(O)=O DJHGAFSJWGLOIV-UHFFFAOYSA-N 0.000 claims description 9
- 229940000488 arsenic acid Drugs 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 229960001755 resorcinol Drugs 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- VJWWIRSVNSXUAC-UHFFFAOYSA-N arsinic acid Chemical class O[AsH2]=O VJWWIRSVNSXUAC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- OQUKIQWCVTZJAF-UHFFFAOYSA-N phenol;sulfuric acid Chemical class OS(O)(=O)=O.OC1=CC=CC=C1 OQUKIQWCVTZJAF-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/66—Arsenic compounds
- C07F9/70—Organo-arsenic compounds
- C07F9/74—Aromatic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE272690C true DE272690C (enExample) | 1900-01-01 |
Family
ID=529223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT272690D Expired DE272690C (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE272690C (enExample) |
-
0
- DE DENDAT272690D patent/DE272690C/de not_active Expired
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1249263B (de) | Verfah ren zur Herstellung vor substituierten 1,3 Dioxocyclopentanderivaten | |
| DE533471C (de) | Verfahren zur Darstellung von Oxydiphenylindolderivaten | |
| DE951626C (de) | Verfahren zur Herstellung von Blei (ó� )-alkoholaten | |
| DE847447C (de) | Verfahren zur Herstellung von 21-Oxypregnen-(5)-ol-(3)-on-(20)-abkoemmlingen | |
| DE203717C (enExample) | ||
| DE553148C (de) | Verfahren zur Darstellung in der Estergruppe basisch substituierter Carbaminsaeure- bzw. Monoalkylcarbaminsaeure- oder Allophansaeureester | |
| DE728360C (de) | Verfahren zur Darstellung einer trisubstituierten Barbitursaeure | |
| DE555004C (de) | Verfahren zur Darstellung von Brenzcatechinarsinsaeuren | |
| DE622405C (de) | Verfahren zur Darstellung ungesaettigter Laktone der alicyclischen Reihe | |
| DE912209C (de) | Verfahren zur Herstellung von 1, 3, 5-Triacetylbenzol | |
| DE303052C (enExample) | ||
| DE258888C (enExample) | ||
| DE730638C (de) | Verfahren zur Herstellung von Phosphoniumverbindungen | |
| DE703342C (de) | ungen der Androstanreihe aus Sterinen | |
| DE959190C (de) | Verfahren zur Herstellung von 2, 4-Dibromallopregnanen | |
| DE1011888B (de) | Verfahren zur Herstellung von Theophyllinderivaten | |
| DE549648C (de) | Verfahren zur Darstellung von Oxalkylcelluloseestern | |
| DE710966C (de) | Verfahren zur Darstellung von Oxycarbonsaeureestern der OEstronreihe | |
| DE875656C (de) | Verfahren zur Darstellung des natuerlichen Oestriols aus Oestron | |
| DE1294967B (de) | Verfahren zur Herstellung von Orcin (3,5-Dihydroxytoluol) | |
| DE531363C (de) | Verfahren zur Darstellung basischer Ester substituierter Chinolin-4-carbonsaeuren | |
| AT157720B (de) | Verfahren zur Herstellung von Glucosiden. | |
| DE941907C (de) | Verfahren zur Herstellung von Diaethylammoniumsalzen substituierter ª‡-Nitrobuttersaeueaethylester | |
| CH181440A (de) | Verfahren zur Darstellung einer phenylierten Verbindung. | |
| DE177054C (enExample) |