Methanol → HCID 178511971, compound

Aniline (5.12 g, 55.0 mmol) was charged into the reaction flask with 100 mL of toluene. This solution was chilled using a wet ice bath. A 2.0 M toluene solution of trimethylaluminum (41.2 mL, 82 mmol) was added dropwise to the chilled reaction mixture over a 15 min period. The cooling bath was removed and the reaction mixture was stirred at room temperature for 2 h. 3-bromobenzonitrile (10.01 g, 55 mmol) was dissolved in 80 mL of toluene and was added dropwise to the reaction mixture. The reaction mixture was then stirred at 75° C. for 18 h. The reaction mixture was cooled to room temperature then was slowing poured into a beaker containing 75 g of silica gel and 150 mL methanol/300 mL DCM. This mixture was stirred at room temperature for 30 min then was filtered through a pad of Celite®. The pad was rinsed with DCM/methanol. The filtrate was stripped under vacuum and the crude residue was triturated with hexanes yielding (E)-3-bromo-N′-phenylbenzimidamide (6.95 g, 25.3 mmol, 45.9%)

1. temperatureThis solution was chilled
2. customThe cooling bath was removed
3. additionwas added dropwise to the reaction mixture
4. stirringThe reaction mixture was then stirred at 75° C. for 18 h
5. temperatureThe reaction mixture was cooled to room temperature
6. additionthen was slowing poured into a beaker
7. stirringThis mixture was stirred at room temperature for 30 min
8. filtrationthen was filtered through a pad of Celite®
9. washThe pad was rinsed with DCM/methanol
10. customthe crude residue was triturated with hexanes

ORD record

ord-1299c86919094389950399ce4cf3c5a5

Source dataset

uspto-grants-2014_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08871361B2