Triacetoxyperiodinane → HCID 59278472, compound

To a solution of 1-(6-bromo-pyridin-3-yl)-propan-1-ol (12.9 g, 59.93 mmol) in THF (200 mL) was added 85% activated MnO2 (6.4 g, 62.57 mmol) and the mixture was stirred overnight. The reaction was monitored by TLC (ethyl acetate-hexanes 4:6) indicating starting material and a new less polar product. To the mixture was added additional 85% activated MnO2 (6.0 g, 58.66 mmol) and the mixture stirred for 2 days. The reaction was monitored by TLC (ethyl acetate-hexanes 3:7) indicting starting material was still present. The mixture was warmed at reflux for 6 hours. The mixture was filtered through diatomaceous earth and concentrated. The residue was diluted with dichloromethane and Dess-Martin periodinane (19 g, 44.8 mmol) was added. After 1 hour, the mixture was diluted with saturated aqueous potassium carbonate (200 mL) and concentrated. The resulting solid was collected by filtration washing with water and dried by pulling vacuum through the filter cake. The solid was then suspended in dichloromethane and filtered and the filtrate was passed through a pad of silica gel eluting with ether to afford 1-(6-bromo-pyridin-3-yl)-propan-1-one as a white solid.

1. stirringthe mixture stirred for 2 days
2. temperatureThe mixture was warmed
3. temperatureat reflux for 6 hours
4. filtrationThe mixture was filtered through diatomaceous earth
5. concentrationconcentrated
6. additionwas added
7. waitAfter 1 hour
8. concentrationconcentrated
9. filtrationThe resulting solid was collected by filtration
10. washwashing with water
11. customdried
12. filtrationfiltered

ORD record

ord-dfe3705ac6e44694b9087fdb8e7d32a5

Source dataset

uspto-grants-2012_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08338610B2