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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490803Generated: November 2, 2026

HCID 178424224, compound → HCID 178423573, compound

https://huagongshe.com/reaction/1490803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178424224HCID 178424224—
ReagentBis(pinacolato)diboraneHCID 2733548—
ReagentTetrabutylazanium {5'-methyl-[2,2'-bipyridin]-5-yl}methanesulfonateHCID 165587889—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178422406HCID 1784224067%
ProductHCID 178423573HCID 17842357374%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F using 2,2,2‐trifluoro‐N‐(3‐(o‐tolyl)propyl)acetamide (61.3 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). 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 13.0:1 meta:para borylation in 86% yield. The crude product was purified by silica gel chromatography (Pet. Ether (40‐60):EtOAc (91:1‐8:1) to give the title compound (as a 10.5:1 mixture of meta:para ratio, as determined by 1 H NMR) as a white solid (74.7 mg, 0.20 mmol, 81%).

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-42ef8ac73afc49c8ab08e8b8ef865d8b
Source noteBorylation dataset from Roche