HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1420142Erstellt: 25. Oktober 2026
Diacetone Alcohol → 2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amine
https://huagongshe.com/reaction/1420142
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diacetone Alcohol | HCID 31256 | — |
| Edukt | Isocyanate | HCID 105034 | — |
| Edukt | 1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzene | HCID 604152 | — |
| Edukt | Di-n-butyldilauryltin | HCID 9809426 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amine | HCID 14716541 | — |
Reaktionsschritte
A flask blanketed with nitrogen was charged with 3-isopropenyl-α,α-dimethylbenzylisocyanate (m-TMI) (475.33 g) and the isocyanate was heated to about 85° C. 4-hydroxy-4-methyl-2-pentanone (274.99 g) was added from an addition funnel to the flask at a fairly rapid rate. The mixture was stirred for two hours and about 0.16 g of dibutyltin dilaurate was added to the mixture, after which the temperature was raised to about 100° C. The reaction mixture was stirred for about 1.5 hours at 100° C. and then allowed to cool and stand at room temperature for approximately 48 hours. Subsequently, about 0.14 g of additional dibutyltin laurate was added and heating at 100° C. was resumed. The reaction mixture temperature was then raised to about 125°-130° C. and the mixture was stirred overnight. Water (800 ml) was added to the cooled reaction mixture and the mixture was distilled. The remaining material in the distillation pot was extracted with toluene. The toluene extract was dried with anhydrous K2CO3, the toluene was distilled and the title product was recovered in a toluene solution.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05889098 |
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| Quelldatensatz | uspto-grants-1999_03 |
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| ORD ID | ord-6d1d573c60624555ab22f358fe230295 |
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| Quellennotiz | uspto-grants-1999_03 |
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