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HRID 1420142作成日:2026年10月27日

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

https://huagongshe.com/reaction/1420142

反応式

関与物質

役割名称HCID仕込み量
反応物Diacetone AlcoholHCID 31256—
反応物IsocyanateHCID 105034—
反応物1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzeneHCID 604152—
反応物Di-n-butyldilauryltinHCID 9809426—
溶媒WaterHCID 962—
生成物2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amineHCID 14716541—

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889098
出典データセットuspto-grants-1999_03
ORD IDord-6d1d573c60624555ab22f358fe230295
出典メモuspto-grants-1999_03