DE91201C - - Google Patents
Info
- Publication number
- DE91201C DE91201C DENDAT91201D DE91201DA DE91201C DE 91201 C DE91201 C DE 91201C DE NDAT91201 D DENDAT91201 D DE NDAT91201D DE 91201D A DE91201D A DE 91201DA DE 91201 C DE91201 C DE 91201C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- naphthalene
- oxy
- disulfonic
- trisulfonic
- 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 21
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 6
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 4
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-Naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 claims description 3
- 239000003518 caustics Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 238000006555 catalytic reaction Methods 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000155 melt Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- GPUMPJNVOBTUFM-UHFFFAOYSA-N naphthalene-1,2,3-trisulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC2=C1 GPUMPJNVOBTUFM-UHFFFAOYSA-N 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-Naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N M-Cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N O-Cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N O-Toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 235000015450 Tilia cordata Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 150000001555 benzenes Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- -1 methyl- Chemical group 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
- C07C65/03—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups monocyclic and having all hydroxy or O-metal groups bound to the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE91201C true DE91201C (it) |
Family
ID=362844
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT91201D Active DE91201C (it) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE91201C (it) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003080542A2 (de) * | 2002-03-22 | 2003-10-02 | Bayer Chemicals Ag | Verfahren zur herstellung von 3-hydroxy-2-methylbenzoesäure |
| EP1371626A2 (de) * | 2002-06-13 | 2003-12-17 | Bayer Aktiengesellschaft | Verfahren zur Herstellung von 3-Alkoxy-2-methylbenzoesäuren |
| EP1371625A1 (de) * | 2002-06-13 | 2003-12-17 | Bayer Aktiengesellschaft | Verfahren zur Herstellung von 3-Acyloxy-2-methylbenzoesäuren |
| US7193092B2 (en) | 2002-08-21 | 2007-03-20 | Lanxess Deutschland Gmbh | Chiral diphosphorus compounds and their transition metal complexes |
-
0
- DE DENDAT91201D patent/DE91201C/de active Active
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003080542A2 (de) * | 2002-03-22 | 2003-10-02 | Bayer Chemicals Ag | Verfahren zur herstellung von 3-hydroxy-2-methylbenzoesäure |
| WO2003080542A3 (de) * | 2002-03-22 | 2004-01-15 | Bayer Chemicals Ag | Verfahren zur herstellung von 3-hydroxy-2-methylbenzoesäure |
| EP1371626A2 (de) * | 2002-06-13 | 2003-12-17 | Bayer Aktiengesellschaft | Verfahren zur Herstellung von 3-Alkoxy-2-methylbenzoesäuren |
| EP1371625A1 (de) * | 2002-06-13 | 2003-12-17 | Bayer Aktiengesellschaft | Verfahren zur Herstellung von 3-Acyloxy-2-methylbenzoesäuren |
| EP1371626A3 (de) * | 2002-06-13 | 2004-07-21 | Bayer Chemicals AG | Verfahren zur Herstellung von 3-Alkoxy-2-methylbenzoesäuren |
| US6891060B2 (en) | 2002-06-13 | 2005-05-10 | Bayeraktiengesellschaft | Preparation of 3-acyloxy-2-methylbenzoic acids |
| US7193092B2 (en) | 2002-08-21 | 2007-03-20 | Lanxess Deutschland Gmbh | Chiral diphosphorus compounds and their transition metal complexes |
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