HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490770Generated: October 30, 2026
HCID 70845390, compound → HCID 178431053, compound
https://huagongshe.com/reaction/1490770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 70845390 | HCID 70845390 | — |
| 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 178431050 | HCID 178431050 | 40% |
| Product | HCID 178431053 | HCID 178431053 | 52% |
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
| DOI | 10.1002/anie.201708967 |
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| Source dataset | Borylation dataset from Roche |
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| ORD ID | ord-2a4e6085cef94ca89a056c2502436433 |
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| Source note | Borylation dataset from Roche |
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