HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490778Generated: October 30, 2026
N-[2-(2-bromophenyl)ethyl]-2,2,2-trifluoroacetamide → HCID 178431043, compound
https://huagongshe.com/reaction/1490778
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-[2-(2-bromophenyl)ethyl]-2,2,2-trifluoroacetamide | HCID 58597272 | — |
| 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 178431027 | HCID 178431027 | 34% |
| Product | HCID 178431043 | HCID 178431043 | 60% |
Reaction Steps
Following general procedure F using 4f (74 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 1:1.7 meta:para borylation in 92% yield. The crude product was purified by silica gel chromatography (15% EtOAc in Petroleum Ether 40‐60 o C) gave the title compound (as a 1:1.8 mixture of meta:para ratio, as determined by 1 H NMR) as a colourless oil (103 mg). A small amount of B2Pin2 impurity was found to be inseparable from the final product on silica. Corrected yield ‐ 100 mg, 0.23 mmol, 94%. 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-c948ea22cf6a42f39e7904366cf4bc1a |
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| Source note | Borylation dataset from Roche |
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