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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490768Generated: October 30, 2026

HCID 18414304, compound → HCID 145913781, compound

https://huagongshe.com/reaction/1490768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18414304HCID 18414304—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 145913781HCID 14591378156%
ProductHCID 178431045HCID 17843104540%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F using 4a (71.3 mg, 0.25 mmol), B2pin2 (127 mg, 0.50 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and dtbpy (2.0 mg, 0.0075 mmol) in THF (1.25 mL). Stirred in vial at 50 °C for 20 hours. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 1.4:1 meta:para borylation in 83% yield. The crude product was purified by silica gel chromatography (10% EtOAc in Petroleum Ether 40‐60 o C) gave the title compound (as a 1.3:1 mixture of meta:para ratio, as determined by 1 H NMR) as a colourless oil (99 mg, 0.24 mmol, 96%). By subtracting the resonances for the meta isomer, the NMR data of the para isomer can be assigned as follows:

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-1ac1e90ccf6e4272bdf693200ec406c6
Source noteBorylation dataset from Roche