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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775395Generated: October 27, 2026

Water → 5,5-dimethyl-5H-indeno[1,2-b]pyridine

https://huagongshe.com/reaction/1775395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant4-AzafluoreneHCID 9205—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product5,5-dimethyl-5H-indeno[1,2-b]pyridineHCID 57872718—

Reaction Conditions

Temperature-10 °C

Reaction Steps

13.5 g (80.7 mmol) of 5H-indeno[1,2-b]pyridine was dissolved in 120 ml dry tetrahydrofuran, and 22.7 g (202 mmol) of potassium tert-butoxide was added to the solution at −10° C. The reaction mixture was maintained at −10° C. for 1 hour. Then the iodomethane 28.7 g (202 mmol) was added dropwise; the solution was then warmed slowly to room temperature and stirred for 6 h. After the reaction completion, water was added to the mixture to terminate the reaction. The reaction mixture was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was evaporated in vacuo, and the residue was crystallized with toluene to give the 5,5-dimethyl-5H-indeno[1,2-b]pyridine, 13.5 g (86%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260363B2
Source datasetuspto-grants-2016_02
ORD IDord-b889ee7e909f460ead1e4d3a19d35bbc
Source noteuspto-grants-2016_02