HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1451991Erstellt: 25. Oktober 2026
Catechol → o-Benzoquinone trimethyl-hexamethylene-diamine
https://huagongshe.com/reaction/1451991
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Catechol | HCID 289 | — |
| Edukt | Oxygen | HCID 977 | — |
| Edukt | N~1~,N~1~,N~6~-Trimethylhexane-1,6-diamine | HCID 15043600 | — |
| Katalysator | Copper sulfate pentahydrate | HCID 24463 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | o-Benzoquinone trimethyl-hexamethylene-diamine | HCID 67706079 | — |
Reaktionsschritte
About 37.93 g (0.24 mol) trimethyl-hexamethylene-diamine and about 0.6 g (0.0024 mol) copper sulfate pentahydrate were dissolved in about 400 mL of methanol. About 26.4 g (0.24 mol) of catechol (chemical name 1,2-dihydroxybenzene) acting as both the quinone precursor and catalyst was added to the reactant mixture. A gentle stream of oxygen at a flow rate of about 50 cc/min was then passed through the reaction mixture for about three hours, while maintaining the reaction temperature around 20°-25 ° C. At the end of three hours the oxygen supply was cut off and the reaction mixture was concentrated under vacuum using a rotary evaporator. The o-benzoquinone-trimethyl-hexamethylene-diamine polymer was precipitated in excess water, washed extensively and dried under vacuum for about 6 hours at a temperature of about 30° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05606010 |
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| Quelldatensatz | uspto-grants-1997_02 |
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| ORD ID | ord-88c5fb0b3da74495b955b38760dc32c3 |
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| Quellennotiz | uspto-grants-1997_02 |
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