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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491482Generated: October 31, 2026

Isoquinoline, 1-(1-naphthalenyl)- → 1-[2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl]isoquinoline

https://huagongshe.com/reaction/1491482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinoline, 1-(1-naphthalenyl)-HCID 3838254—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
Product1-[2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl]isoquinolineHCID 1015479340%

Reaction Conditions

Temperature25 °C

Reaction Steps

Following the general procedure, column chromatography (EtOAc/nhexane 1:3) afforded 9a (160 mg, 84 %) as a light yellow solid. Evaporation from EtOAc/n-hexane afforded X-Ray quality crystals.

Provenance & Evidence

DOI10.1002/anie.201104544
Source datasetBorylation dataset from Roche
ORD IDord-2c50d19136e04b4faec80b4df30a9add
Source noteBorylation dataset from Roche