HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490764Generated: October 30, 2026
HCID 63789239, compound → HCID 123498283, compound
https://huagongshe.com/reaction/1490764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 63789239 | HCID 63789239 | — |
| 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 123498283 | HCID 123498283 | 60% |
| Product | HCID 178453018 | HCID 178453018 | 38% |
Reaction Steps
Following general procedure F using tert‐butyl (2‐(trifluoromethyl)benzyl)carbamate (68.8 mg, 0.25 mmol), B2pin2 (95 mg, 0.375 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and dtbpy (2.0 mg, 0.0075 mmol) in THF (1.25 mL). The reaction was stirred at 50 °C for 20 hours before cooling and the solvents removed. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 1:1.6 meta:para borylation in 98% yield. As the para isomer could be characterised from the reaction with 1a the product was not isolated.
Provenance & Evidence
| DOI | 10.1002/anie.201708967 |
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| Source dataset | Borylation dataset from Roche |
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| ORD ID | ord-1c8694c62b8b46008040a43e875704ba |
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| Source note | Borylation dataset from Roche |
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