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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419442Generated: October 25, 2026

Diacetone Alcohol → 2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amine

https://huagongshe.com/reaction/1419442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiacetone AlcoholHCID 31256—
ReactantIsocyanateHCID 105034—
Reactant1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzeneHCID 604152—
ReactantDi-n-butyldilauryltinHCID 9809426—
SolventWaterHCID 962—
Product2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amineHCID 14716541—

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886116
Source datasetuspto-grants-1999_03
ORD IDord-01b01321ea694d99be6dbba81af705ea
Source noteuspto-grants-1999_03