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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160031Generated: November 2, 2026

Indole → 2-Phenylpyridine

https://huagongshe.com/reaction/1160031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantTolueneHCID 1140—
ReactantSodium t-butoxideHCID 23676156—
Reactant2-(2,4-Difluorophenyl)-4-chloropyridineHCID 68645902—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
SolventDichloromethaneHCID 6344—
Product2-PhenylpyridineHCID 13887126%

Reaction Steps

44.9 mg (0.2 mmol) of palladium acetate, 70 mg (0.2 mmol) of 2-(dicyclohexylphosphino)biphenyl, 1.3455 grams (14 mmol) of sodium t-butoxide, 1.1281 grams (5 mmol) of 2-(2,4-difluorophenyl)-4-chloropyridine, and 0.7029 grams (6 mmol) of indole were mixed with 60 ml of toluene and refluxed for 48 hours. Next a double portion of the catalyst package and one more portion of indole was added to the mixture to reflux for 72 hours. The reaction contents were cooled to room temperature, diluted with dichloromethane and preabsorbed onto silica and chromatographed using methylene chloride eluent to isolate 0.978 grams of yellow solid in 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816016B1
Source datasetuspto-grants-2010_10
ORD IDord-23c56ae5a265462d94daf1039cd93230
Source noteuspto-grants-2010_10