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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490816Generated: October 30, 2026

HCID 178521919, compound → HCID 178431004, compound

https://huagongshe.com/reaction/1490816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178521919HCID 178521919—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431004HCID 17843100437%
ProductHCID 178431031HCID 17843103135%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F usin trans‐12a  (67.8 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 1:1.4:1.3 meta:dimeta:para borylation (overall meta:para ratio of 1.8:1) in 98% 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 1:1.3:1.2 meta:dimeta:para ratio or overall meta:para ratio of 1.9:1, as determined by 1 H NMR) as a white solid (104.3 mg, 0.24 mmol, 94%). The mass quoted above is the actual mass of the isolated mixture of products, whilst the amount of substance in mmol has been calculated by examining the ratios of the dimeta to monoborylated products and accounting for the extra mass due to the higher molecular weight of the dimeta product. By subtracting the resonances for the meta isomer, the NMR data of the dimeta and para isomer can be assigned as follows:

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-a50b47f31a74420f8d51373fe2d335d7
Source noteBorylation dataset from Roche