HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490768Generated: October 30, 2026
HCID 18414304, compound → HCID 145913781, compound
https://huagongshe.com/reaction/1490768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18414304 | HCID 18414304 | — |
| Reagent | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reagent | 4,4'-Di-tert-butyl-2,2'-bipyridyl | HCID 4249187 | — |
| Catalyst | Bis(1,5-cyclooctadiene)dimethoxydiiridium | HCID 76001521 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 145913781 | HCID 145913781 | 56% |
| Product | HCID 178431045 | HCID 178431045 | 40% |
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
| DOI | 10.1002/anie.201708967 |
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| Source dataset | Borylation dataset from Roche |
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| ORD ID | ord-1ac1e90ccf6e4272bdf693200ec406c6 |
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| Source note | Borylation dataset from Roche |
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