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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713584Generated: November 4, 2026

10-phenyl-1H-indeno[1,2-b]quinolin-11-one → 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol

https://huagongshe.com/reaction/713584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant10-phenyl-1H-indeno[1,2-b]quinolin-11-oneHCID 131734054—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-olHCID 11760624890%

Reaction Steps

After dripping 1M phenylmagnesium bromide (20 ml, 20.0 mmol) into the starting material 10-phenyl-1H-indeno[1,2-b]quinolin-11-one (3.07 g, 10.0 mmol) which is dissolved in pure tetrahydrofuran, the mixed solution undergoes reaction for 24 hours at room temperature. Then, the reaction is terminated by adding ammonium chloride solution therein. Finally, 3.47 g of 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol is obtained by filtering the mixed solution to remove precipitates. The percentage yield is 90.0%. 10-diphenyl-11H-indeno[1,2-b]quinolin-11-ol obtained here can be also used as starting materials to produce other 6H-indeno[2,1-b]quinoline derivatives.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184396B2
Source datasetuspto-grants-2015_11
ORD IDord-594abf8213c144a6941230de9c1dd7e9
Source noteuspto-grants-2015_11