HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1288403Erstellt: 26. Oktober 2026
Carbon Disulfide → Antimony N-(2-octyl)-N-ethyldithiocarbamate
https://huagongshe.com/reaction/1288403
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Oxo(oxostibanyloxy)stibane | HCID 27652 | — |
| Edukt | 1-Heptanamine, 1-methyl, N-ethyl | HCID 525053 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Antimony N-(2-octyl)-N-ethyldithiocarbamate | HCID 21501793 | — |
Reaktionsschritte
In a 3-liter, three-neck, round-bottom flask equipped with a stirrer, thermometer, dropping funnel and condenser was placed 157 g. (grams) (1.0 mole) of N-(2-octyl)-N-ethylamine, 49 g. (0.168 mole) of antimony trioxide and 1000 ml. (milliliters) of hexane. The stirred mixture was heated to reflux (68°C.) and 80 g. (1.05 moles) of carbon disulfide was added over a period of 1 hour. The mixture was stirred at reflux for an additional 3 hours, and then the water generated during the reaction was azeotroped off (9 ml.). The mixture was filtered hot in order to remove any unreacted antimony oxide. The hexane solution was cooled to room temperature and the hexane was then removed at reduced pressure. A viscous oil was isolated having an Index of refraction ND22 =1.627.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03988249 |
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| Quelldatensatz | uspto-grants-1976_10 |
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| ORD ID | ord-ee4a5f3811d6448da4ab0885712207dd |
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| Quellennotiz | uspto-grants-1976_10 |
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