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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363257생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/363257

반응식

참여 물질

역할이름HCID투입량
반응물Diacetone AlcoholHCID 31256—
반응물IsocyanateHCID 105034—
반응물1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzeneHCID 604152—
반응물Di-n-butyldilauryltinHCID 9809426—
용매WaterHCID 962—
생성물2-(3-(Prop-1-en-2-yl)phenyl)propan-2-amineHCID 14716541—

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05872297
출처 데이터셋uspto-grants-1999_02
ORD IDord-049790ef22324535a49d62db3b81ed70
출처 메모uspto-grants-1999_02