戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 896736作成日:2026年10月26日

Ammonia → 1-(8-Quinolyl)-2-methylindene

https://huagongshe.com/reaction/896736

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物2-MethylindanoneHCID 249262—
反応物2-BromoquinolineHCID 2762756—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(8-Quinolyl)-2-methylindeneHCID 2197797745%

反応条件

温度80 °C

反応手順

6.70 ml of n-BuLi (16.8 mmol) was added dropwise at 100° C. to a solution of 3.50 g of o-bromoquinoline (16.8 mmol) in 50 ml of THF, and the mixture was stirred for 15 minutes at 80° C. Next, a solution of 50 ml of THF and 2.45 g of 2- methyl-1-indanone (16.8 mmol) was added within ten minutes to the lithiated bromoquinoline. The solution was left to return to room temperature, and subsequently boiled for three hours in reflux. After cooling to room temperature, ice was added and the mixture was acidified to pH 1 with hydrochloric acid, and subsequently heated under relfux for three hours. The reaction mixture was adjusted with ammonia solution to pH 9, and the aqueous phase was extracted with diethyl ether. The combined organic phases were dried, and the solvent was removed. The raw product was purified by distillation in a vacuum at 150 to 160° C. and 10−2 mbar. 1.5 g of 1-(8-quinolyl)-2-methylindene (45%) were obtained in the form of a viscous yellow resin.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06919412B1
出典データセットuspto-grants-2005_07
ORD IDord-f9422e90423f495bbd3a461ef7b1750d
出典メモuspto-grants-2005_07