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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490807Generated: November 1, 2026

HCID 178423712, compound → HCID 178423698, compound

https://huagongshe.com/reaction/1490807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178423712HCID 178423712—
ReagentBis(pinacolato)diboraneHCID 2733548—
ReagentTetrabutylazanium {5'-methyl-[2,2'-bipyridin]-5-yl}methanesulfonateHCID 165587889—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178423658HCID 1784236589%
ProductHCID 178423698HCID 17842369883%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F using 2,2,2‐trifluoro‐N‐(3‐(4'‐methyl‐[1,1'‐biphenyl]‐2‐ yl)propyl)acetamide (80.3 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 10.4:1 meta:para borylation in 99% yield. The crude product was purified by silica gel chromatography (Pet. Ether (40‐60):EtOAc (19:1‐9:1) to give the title compound (as a 9.5:1 mixture of meta:para ratio, as determined by 1 H NMR) as a white solid (102.4 mg, 0.23 mmol, 92%).

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-7a7ce259d48648448218c44b7d39ce2e
Source noteBorylation dataset from Roche