HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1730992Erstellt: 24. Oktober 2026
1-Bromohexane → 5-n-Hexylthio 4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thione
https://huagongshe.com/de/reaction/1730992
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromohexane | HCID 8101 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 5-Mercapto-4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thione | HCID 21494630 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-n-Hexylthio 4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thione | HCID 9868594 | — |
Reaktionsschritte
0.92 parts of sodium was dissolved in 80 parts of ethanol and to this was added 14.8 parts of 5-mercapto-4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thione, as prepared in example 11 dissolved in 200 parts ethanol. The mixture was then warmed to 50°C and a solution of 6.6 parts n-hexyl bromide in 50 parts ethanol was added dropwise. The mixture was refluxed for 5 hours, the ethanol evaporated, and the residue extracted with diethyl ether. Evaporation of the ether solution gave a crystalline residue which was crystallised from ether to give 12 parts of 5-n-hexylthio 4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thione, m.p. 110°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03994923 |
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| Quelldatensatz | uspto-grants-1976_11 |
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| ORD ID | ord-0255547498fd49348e78a655574d2eca |
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| Quellennotiz | uspto-grants-1976_11 |
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