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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1760066생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1760066

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) were added dropwise at 100° C. to 3.50 g of o-bromoquinoline (16.8 mmol) dissolved in 50 ml of THF, and the mixture was subsequently stirred at 80° C. for 15 minutes. A solution of 50 ml of THF and 2.45 g of 2-methyl-1-indanone (16.8 mmol) was then added to the lithiated bromoquinoline over the course of 10 minutes. The mixture was allowed to cool to room temperature, and the solution was then refluxed for three hours, cooled to room temperature, acidified to pH 1 using ice and hydrochloric acid and subsequently refluxed for three hours. The reaction mixture was adjusted to pH 9 using ammonia solution, and the aqueous phase was extracted with diethyl ether. The combined organic phases were dried, and the solvent was removed. The crude product was purified by distillation under reduced pressure at 150-160° C./10−2 mbar, giving 1.5 g of 1-(8-quinolyl)-2-methylindene (45%) as a yellow, viscous resin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06838563B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-95497ed6fb94459cbc7bf6a38e1b990a
출처 메모uspto-grants-2005_01