CH126718A - Process for the preparation of 1,5-dichloro-2,6-dimethylnaphthalene. - Google Patents
Process for the preparation of 1,5-dichloro-2,6-dimethylnaphthalene.Info
- Publication number
- CH126718A CH126718A CH126718DA CH126718A CH 126718 A CH126718 A CH 126718A CH 126718D A CH126718D A CH 126718DA CH 126718 A CH126718 A CH 126718A
- Authority
- CH
- Switzerland
- Prior art keywords
- dimethylnaphthalene
- dichloro
- preparation
- heated
- sulfuryl chloride
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von 1.6-Dichlor-2.6-dimethylnaphtalin. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung von 1.5-Dichlor- 2. 6-dimethylnaphtalin.
Das Verfahren ist dadurch gekennzeichnet, dass man auf 1 Mol. 2.6-Dimethylnaphtalin 2 Mol. Sulfurylchlorid bei mässiger Tempe ratur einwirken lässt. Es kann ohne Lösungs mittel oder auch mit indifferenten Lö8ungs- mitteln wie Äther, Tetrachlormethan usw. ausgeführt werden. Die Temperatur wird vorteilhaft unter 65 gehalten. Das 1. 5-Dichlor- 2.6-Dimethylnaphtalin soll zur Herstellung von Farbstoffen Verwendung finden.
<I>Beispiel</I> 156 Gewichtsteile 2.6-Di-nethylnaphtalin werden mit 270 Gewichtsteilen Sulfurylchlorid gemischt und auf 30-40 erwärmt. 170 Ge wichtsteile des Endproduktes destillieren von<B>328-3330</B> (unkorr.) und erstarren sofort in der Vorlage zu weissen Prismen. Aus Alkohol oder Eisessig umkristallisiert, schmel- zen sie scharf bei 130 und stellen einheit liches 1.5-Dichlor-2.6-Dimethyln a'phtalin dar, das einen angenehmen, schwach aromatischen Geruch hat.
In Chloroform ist es sehr leicht löslich; Äther, Ligroin, aromatische Kohlen wasserstoffe, Methyl- und Äthylalkohol, so wie Eisessig sind geeignete Kristallisations- mittel.
In konzentrierter Schwefelsäure löst es sich kalt kaum, beim Erhitzen tritt unter Dunkelfärbung Schwefeldioxyd-Entwicklung und Oxydation ein.
Process for the preparation of 1,6-dichloro-2,6-dimethylnaphthalene. The subject of this additional patent is a process for the preparation of 1,5-dichloro-2,6-dimethylnaphthalene.
The process is characterized in that 2 moles of sulfuryl chloride are allowed to act on 1 mole of 2,6-dimethylnaphthalene at a moderate temperature. It can be carried out without solvents or with inert solvents such as ether, carbon tetrachloride, etc. The temperature is advantageously kept below 65. The 1. 5-dichloro-2,6-dimethylnaphthalene is said to be used for the production of dyes.
<I> Example </I> 156 parts by weight of 2,6-dimethylnaphthalene are mixed with 270 parts by weight of sulfuryl chloride and heated to 30-40. 170 parts by weight of the end product distill <B> 328-3330 </B> (uncorrected) and solidify immediately in the original to form white prisms. Recrystallized from alcohol or glacial acetic acid, they melt sharply at 130 and are uniform 1,5-dichloro-2,6-dimethyln a'phtalin, which has a pleasant, slightly aromatic odor.
It is very easily soluble in chloroform; Ether, ligroin, aromatic hydrocarbons, methyl and ethyl alcohol and glacial acetic acid are suitable crystallization agents.
In concentrated sulfuric acid it hardly dissolves when cold; when heated, the development of sulfur dioxide and oxidation occurs with a dark color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE126718X | 1925-12-29 | ||
CH125470T | 1926-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH126718A true CH126718A (en) | 1928-07-02 |
Family
ID=25710465
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH126718D CH126718A (en) | 1925-12-29 | 1926-12-27 | Process for the preparation of 1,5-dichloro-2,6-dimethylnaphthalene. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH126718A (en) |
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1926
- 1926-12-27 CH CH126718D patent/CH126718A/en unknown
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