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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490770Generated: October 30, 2026

HCID 70845390, compound → HCID 178431053, compound

https://huagongshe.com/reaction/1490770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70845390HCID 70845390—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431050HCID 17843105040%
ProductHCID 178431053HCID 17843105352%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F using 4b (66.8 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 1.3:1 meta:para borylation in 97% yield. The crude product was purified by silica gel chromatography (40% EtOAc in Petroleum Ether 40‐60 o C) gave the title compound (as a 1.2:1 mixture of meta:para ratio, as determined by 1 H NMR) as a colourless oil (90 mg, 0.23 mmol, 92%). 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-2a4e6085cef94ca89a056c2502436433
Source noteBorylation dataset from Roche