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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227857Generated: October 26, 2026

Indole → N-(4-methylphenyl)indole

https://huagongshe.com/reaction/227857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant4-BromotolueneHCID 7805—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-(4-methylphenyl)indoleHCID 979428694%

Reaction Conditions

Temperature100 °C

Reaction Steps

An oven-dried resealable Schlenk tube was purged with argon and charged with Pd2(dba)3 (11.2 mg, 0.012 mmol, 2.5 mol % Pd), 2 [Example 1] (14.4 mg, 0.036 mmol, 7.5 mol %), NaOt-Bu (130 mg, 1.35 mmol) and indole (115 mg, 0.98 mmol). The tube was purged with argon then toluene (1.0 mL) and 4-bromotoluene (120 μL, 0.98 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at 100° C. for 21 h. The reaction was then diluted with ether (20 mL), filtered through celite and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel to afford 191 mg (94%) of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560582B2
Source datasetuspto-grants-2009_07
ORD IDord-5d4279b50360464c9a98c95f333ddb4e
Source noteuspto-grants-2009_07