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

温度

100 °C

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.

1. customA flask blanketed with nitrogen
2. stirringThe reaction mixture was stirred for about 1.5 hours at 100° C.
3. temperatureto cool
4. waitstand at room temperature for approximately 48 hours
5. temperatureheating at 100° C.
6. temperatureThe reaction mixture temperature was then raised to about 125°-130° C.
7. stirringthe mixture was stirred overnight
8. distillationthe mixture was distilled
9. distillationThe remaining material in the distillation
10. extractionpot was extracted with toluene
11. extractionThe toluene extract
12. dry with materialwas dried with anhydrous K2CO3
13. distillationthe toluene was distilled
14. customthe title product was recovered in a toluene solution

ORDレコード

ord-049790ef22324535a49d62db3b81ed70

出典データセット

uspto-grants-1999_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05872297