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HRID 373579作成日:2026年10月25日

Citric Acid → 3-Butyl-7-(2,5-dimethylbenzyl)-9, 9-dimethyl-3,7-diazabicyclo[3,3,1]nonane

https://huagongshe.com/reaction/373579

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Lithium amideHCID 24532—
反応物Benzene, 2-(chloromethyl)-1,4-dimethyl-HCID 69987—
反応物HCID 14369008HCID 14369008—
溶媒DimethylformamideHCID 6228—
生成物3-Butyl-7-(2,5-dimethylbenzyl)-9, 9-dimethyl-3,7-diazabicyclo[3,3,1]nonaneHCID 15745308—

反応条件

温度60 °C

反応手順

3.5 g 3-n-butyl-9,9-dimethyl-3, 7-diazabicyclo[3,3,1]nonane were dissolved in 25 ml of dimethyl formamide, and 0.8 g of lithium amide was added to the solution. The reaction mixture was then maintained at a temperature of 60° C. for 1 hour and subsequently allowed to cool. After cooling, a solution of 5.6 g of 2,5-dimethylbenzyl chloride in 10 ml of dimethyl formamide was added dropwise, and the reaction mixture was stirred for a further 4 hours at 80° C. Then aqueous citric acid solution was added to the reaction mixture in order to dissolve the title compound as a citric acid salt. The solution was washed with diethyl ether and then rendered alkaline by adding dilute sodium hydroxide solution, whereupon the title compound was again freed as a base. The free base was extracted with diethyl ether. After the ether extract was dried over magnesium sulfate, the ether solution was filtered, and the ether was distilled off. The remaining oil was purified by distillation in a bulb tube at 210° C. and 0.01 Torr.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05164401
出典データセットuspto-grants-1992_11
ORD IDord-8ff9bd8605bb45d18e2451b432d0c145
出典メモuspto-grants-1992_11