AT69743B - Process for the preparation of 2.4.6.2'.4'.6'-hexanitrodiphenyl sulfide. - Google Patents
Process for the preparation of 2.4.6.2'.4'.6'-hexanitrodiphenyl sulfide.Info
- Publication number
- AT69743B AT69743B AT69743DA AT69743B AT 69743 B AT69743 B AT 69743B AT 69743D A AT69743D A AT 69743DA AT 69743 B AT69743 B AT 69743B
- Authority
- AT
- Austria
- Prior art keywords
- preparation
- sulfide
- hexanitrodiphenyl
- hexanitrodiphenyl sulfide
- desc
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 239000002535 acidifier Substances 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 4
- 239000002360 explosive Substances 0.000 description 2
- OKWLCUWJPPORKE-UHFFFAOYSA-N 1,2,3,4,5-pentanitro-6-(2-nitrophenyl)sulfanylbenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1SC1=C([N+]([O-])=O)C([N+]([O-])=O)=C([N+]([O-])=O)C([N+]([O-])=O)=C1[N+]([O-])=O OKWLCUWJPPORKE-UHFFFAOYSA-N 0.000 description 1
- SRYLRVUJDQTFDL-UHFFFAOYSA-N 1-chloro-2,3,4-trinitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1[N+]([O-])=O SRYLRVUJDQTFDL-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung von 2.4. 6. 2'. 4'. 6'-Hexanitrodiphenylsulfid.
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ergibt sehr vint, ; tinte und schlechte Ausbeuten. Eine bessere Darstellungsweise, und zwar für das 2. 4. 2'. 4'-Tetramtrodiphenylsulfid, ist aus dem D. R. P. Nr. 94077 bekannt geworden.
Die daselbst beschriebene Methode beruht auf der Umsetzung von 2 Molekülen l-Chlor-2. 4-dinitrohenzol mit 2 Molekülen Thiosulfat nach der Gleichung :
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Es wurde nun gefunden, dass man die Hexaverbindung darstellen kann. wenn man an Stelle von 2 Molekülen Thiosulfat nur l Molekül Thiosulfat auf 2 Moleküle Chlortrinitrobenzol ein-
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waschen und getrocknet. Die Ausbeute beträgt etwa 90% der Theorie.
Man erhält ein rein gelbes Produkt vom Schmelzpunkt 226 und den in der Literatur an- gegebenen, bekannten Eigenschaften. Jeder geringe Überschuss von Thiosulfat ruft dagegen eine sich durch Dunkelfärbung kennzeichnende Zersetzung hervor.
Das Hexanitrodiphenylsulfid besitzt explosive Eigenschaften und soll daher in der Sprengstofftechnik Verwendung finden.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Procedure for the presentation of 2.4. 6. 2 '. 4 '. 6'-hexanitrodiphenyl sulfide.
EMI1.1
results in very vint,; ink and poor yields. A better way of representing, for the 2nd 4th 2 '. 4'-Tetramtrodiphenyl sulfide is known from D. R. P. No. 94077.
The method described there is based on the conversion of 2 molecules of l-chloro-2. 4-dinitrohenzene with 2 molecules of thiosulphate according to the equation:
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It has now been found that the hexa compound can be produced. if instead of 2 molecules of thiosulfate only 1 molecule of thiosulfate is used for 2 molecules of chlorotrinitrobenzene
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wash and dry. The yield is about 90% of theory.
A purely yellow product with a melting point of 226 and the known properties given in the literature is obtained. Any slight excess of thiosulphate, on the other hand, causes decomposition, which is characterized by a dark color.
Hexanitrodiphenyl sulfide has explosive properties and should therefore be used in explosives technology.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE69743X | 1912-08-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT69743B true AT69743B (en) | 1915-08-25 |
Family
ID=5635146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT69743D AT69743B (en) | 1912-08-27 | 1913-07-21 | Process for the preparation of 2.4.6.2'.4'.6'-hexanitrodiphenyl sulfide. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT69743B (en) |
-
1913
- 1913-07-21 AT AT69743D patent/AT69743B/en active
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