N-bromobutanimide → HCID 57963064, compound

Participants

Reaction Steps

To (6-fluoro-pyridin-2-yl)-(4-methoxy-benzyl)-amine (78, 151 g, 650 mmol) in 4 L of acetonitrile under nitrogen, N-bromosuccinimide (116 g, 650 mmol) was added in portions. After reacting for 2 hours, the solvent was removed under vacuum and the residue taken up in ethyl acetate, then poured into aqueous sodium thiosulfate. The organic layer was washed with warm water, dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was crystallized from heptane to provide the desired compound (79, 172 g, 553 mmol, 85% yield).

Provenance & Evidence