戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 26003作成日:2026年10月26日

Sodium Bicarbonate → 1-(3,4-Dihydroxyphenyl)-2-((1-methylethyl)amino)ethanone

https://huagongshe.com/reaction/26003

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Isoproterenone hydrochlorideHCID 2830496—
溶媒WaterHCID 962—
生成物1-(3,4-Dihydroxyphenyl)-2-((1-methylethyl)amino)ethanoneHCID 8465—

反応手順

4-(isopropylaminoacetyl)catechol hydrochloride (34 g.) is dissolved in 60 ml. of water and the aqueous solution is made alkaline with an aqueous saturated sodium hydrogen carbonate solution. The resulting alkaline solution is extracted with chloroform. Upon removal of the chloroform by distillation, crude 4-(isopropylaminoacetyl)catechol is obtained. The crude product is purified by recrystallization from benzene-petroleum ether. 20.9 g. of 4-(isopropylaminoacetyl)catechol and 10.2 g. of methylene chloride are dissolved in 20 ml. of methanol and the resulting solution is placed in a glass pressure reactor together with 3 g. of Tobin bronze shavings. An additional 40 ml. of methanol are added to the solution and the reactor is cooled with ice. An ice cold aqueous KOH solution (consisting of 11 g. of KOH and 15 ml. of water) is added thereto dropwise with stirring and, after the addition is complete, the reactor is sealed. The reaction is carried out with stirring at 100°-110° C. for 18 hours. After the reaction is complete, the methanol is distilled of under reduced pressure. The residual aqueous alkaline solution is mixed with 100 ml. of water and then extracted with ether. The ether extract is washed with 1N KOH and water and then dried. Upon distillation of the ether, crude α-isopropylamino-(3,4-methylenedioxy)acetophenone is obtained. Upon recrystallization of the crude product from benzene-petroluem ether, 8.2 g. of crystalline α-isopropylamino-(3,4-methylenedioxy)acetophenone are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147799
出典データセットuspto-grants-1979_04
ORD IDord-8d627295713e4d3eb231d5815ad50800
出典メモuspto-grants-1979_04