CH85227A - Process for the preparation of ethylbenzylaniline-3,4'-disulfonic acid. - Google Patents
Process for the preparation of ethylbenzylaniline-3,4'-disulfonic acid.Info
- Publication number
- CH85227A CH85227A CH85227DA CH85227A CH 85227 A CH85227 A CH 85227A CH 85227D A CH85227D A CH 85227DA CH 85227 A CH85227 A CH 85227A
- Authority
- CH
- Switzerland
- Prior art keywords
- disulfonic acid
- ethylbenzylaniline
- preparation
- acid
- mol
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000003756 stirring Methods 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
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/46—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
EMI0001.0001
Verfahren <SEP> zur <SEP> Heratellung <SEP> von <SEP> Äthylbenzylanilin-3.4'-dihulfosäure. Es wurde gefunden, dah man die Äthyl- benzylariilin-3.4'-disulfosäure in technisch schi- vorteilhafter Weise durch Kondensation von 1 Dlol. benzylchlorid-p-sulfosaureni Natrium mit 1 Mol. Monoätbvlmetanilsäure in wäs seriger Lösung darstellen kann.
Man erhält eine Lösung, welche ohne weiteres zur Her stellung von Farbstoffen verwendet werden kann, oder aus welcher die Äthylbeiizylaiiilin- 3#4'-disulfosäure nach bekannten Methoden isoliert werden kann. <I>Beispiel:</I> 33,5 kg bloiioäthylmetanilsaiires Natrium werden in 200 Liter Wasser gelöst und bei <B>700</B> unter Rühren nacheinander mit 11 kg Soda und 45 kg benzylclilorid-p-sulfosaui-em -Natrium versetzt. Wenn alles eingetragen ist, wird während einer Viertelstunde gekocht, wobei die Unisetzung quantitativ vor sich geht.
EMI0001.0001
Method <SEP> for the <SEP> production <SEP> of <SEP> ethylbenzylaniline-3,4'-dihulfonic acid. It has been found that ethylbenzylariline-3,4'-disulfonic acid can be obtained in a technically advantageous manner by condensation of 1 Dlol. benzylchloride-p-sulfosaureni sodium with 1 mol. Monoätbvlmetanilicäure in aqueous solution can represent.
A solution is obtained which can readily be used for the preparation of dyes, or from which the Äthylbeiizylaiiilin- 3 # 4'-disulfonic acid can be isolated by known methods. <I> Example: </I> 33.5 kg of bloiioäthylmetanilsaiires sodium are dissolved in 200 liters of water and at <B> 700 </B> with stirring in succession with 11 kg of soda and 45 kg of benzyl chloride-p-sulfosaui-em-sodium offset. When everything has been entered, it is cooked for a quarter of an hour, the unisposition being done quantitatively.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH85227T | 1916-01-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH85227A true CH85227A (en) | 1920-06-01 |
Family
ID=4341511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH85227D CH85227A (en) | 1916-01-19 | 1916-01-19 | Process for the preparation of ethylbenzylaniline-3,4'-disulfonic acid. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH85227A (en) |
-
1916
- 1916-01-19 CH CH85227D patent/CH85227A/en unknown
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