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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005643Generated: October 25, 2026

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

https://huagongshe.com/reaction/1005643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant2-MethylindanoneHCID 249262—
Reactant2-BromoquinolineHCID 2762756—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(8-Quinolyl)-2-methylindeneHCID 2197797745%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787498B2
Source datasetuspto-grants-2004_09
ORD IDord-f4b34a6256b6471b9743b9db0fd5b253
Source noteuspto-grants-2004_09