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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198242Generated: October 31, 2026

Triacetoxyperiodinane → HCID 59278472, compound

https://huagongshe.com/reaction/2198242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 86640808HCID 86640808—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
ProductHCID 59278472HCID 59278472—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-dfe3705ac6e44694b9087fdb8e7d32a5
Source noteuspto-grants-2012_12