HCID 87773595, compound → HCID 178431058, compound

Participants

Reaction Conditions

Reaction Steps

Following general procedure F using N‐(3‐(2‐chlorophenyl)propyl)‐2,2,2‐trifluoroacetamide (66.4 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 10:78:10 dimeta:meta:para borylation in 98% 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 7:78:10 mixture of dimeta:meta:para ratio, as determined by 1 H NMR) as a colourless oil (97.1 mg, 0.24 mmol, 97%*).

Provenance & Evidence