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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355669Generated: October 31, 2026

Potassium Hydroxide → 6-Bromo-1-naphthalen-1-ylmethyl-3,3-bis-pyridin-4-ylmethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1355669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
Reactant6-Bromo-1-naphthalen-1-ylmethyl-1,3-dihydro-indol-2-oneHCID 18507769—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-1-naphthalen-1-ylmethyl-3,3-bis-pyridin-4-ylmethyl-1,3-dihydro-indol-2-oneHCID 1850776247.3%

Reaction Steps

6-Bromo-1-naphthalen-1-ylmethyl-1,3-dihydro-indol-2-one (195 mg, 0.554 mmol) was dissolved in 1 ml of THF and was then added to a previously degassed solution of 3 ml of THF and 5 ml of aqueous 1 N KOH under an atmosphere of dry N2. To this solution was added 4-picolyl chloride hydrochloride (275 mg, 1.67 mmol). The reaction mixture was then stirred at ambient temperature for 2 hours after which time the reaction mixture was concentrated under vacuum to give a green oil. The oil was partitioned between DCM and saturated aqueous NaHCO3. The DCM layer was then washed with brine, dried over Na2SO4, filtered and concentrated under vacuum to give a dark oil which was chromatographed on flash silica gel eluting with a gradient from EtOAc/hexanes (50:50) to EtOAc to EtOAc/MeOH (95:5) to give 140 mg of the titled compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586447B1
Source datasetuspto-grants-2003_07
ORD IDord-bd3a14a7105340a093c0feae8f98b08d
Source noteuspto-grants-2003_07