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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromohexaneHCID 8101—
EduktSodiumHCID 5360545—
Edukt5-Mercapto-4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thioneHCID 21494630—
LösungsmittelEthanolHCID 702—
Produkt5-n-Hexylthio 4-(3,5-di-t-butyl-4-hydroxyphenyl)-1,2-dithiole-3-thioneHCID 9868594—

Reaktionsbedingungen

Temperatur50 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03994923
Quelldatensatzuspto-grants-1976_11
ORD IDord-0255547498fd49348e78a655574d2eca
Quellennotizuspto-grants-1976_11