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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896736생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/896736

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물2-MethylindanoneHCID 249262—
반응물2-BromoquinolineHCID 2762756—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(8-Quinolyl)-2-methylindeneHCID 2197797745%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06919412B1
출처 데이터셋uspto-grants-2005_07
ORD IDord-f9422e90423f495bbd3a461ef7b1750d
출처 메모uspto-grants-2005_07