HCID 69080912, compound → HCID 86695610, compound

Participants

Reaction Steps

A solution of (3-chloro-5-(pyridin-2-yl)phenyl)methanol (116 mg; 0.64 mmol) in anh. THF (6 ml) was treated with MnO2 (877 mg; 10.09 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 6.5 h. The resulting reaction mixture was then filtered over celite, and the separated solids were washed with THF. The filtrate was concentrated to dryness under reduced pressure giving 3-chloro-5-(pyridin-2-yl)benzaldehyde as a yellow oil. LC-MS (conditions A): tR=0.43 min.; no ionisation.

Provenance & Evidence