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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490777Generated: October 29, 2026

N-[2-(2-bromophenyl)ethyl]-2,2,2-trifluoroacetamide → HCID 178431027, compound

https://huagongshe.com/reaction/1490777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(2-bromophenyl)ethyl]-2,2,2-trifluoroacetamideHCID 58597272—
ReagentBis(pinacolato)diboraneHCID 2733548—
ReagentTetrabutylazanium {5'-methyl-[2,2'-bipyridin]-5-yl}methanesulfonateHCID 165587889—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431027HCID 17843102780%
ProductHCID 178431043HCID 17843104311%

Reaction Conditions

Temperature50 °C

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 1a (3.8 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 8.0:1 meta:para borylation in 93% 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 7.2:1 mixture of meta:para ratio, as determined by 1 H NMR) as a white solid (103 mg). A small amount of B2Pin2 impurity was found to be inseparable from the final product on silica. Corrected yield ‐ 96 mg, 0.23 mmol, 91%.

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-cfea1f62d1754743bf73d823c2bbee3c
Source noteBorylation dataset from Roche