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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749986Generated: October 28, 2026

Triacetoxyperiodinane → Tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1749986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
Reactanttert-Butyl 4-(3-hydroxypropyl)tetrahydro-1(2h)-pyridinecarboxylateHCID 2800739—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(3-oxopropyl)piperidine-1-carboxylateHCID 1065774588.1%

Reaction Steps

A solution of tert-butyl 4-(3-hydroxypropyl)piperidine-1-carboxylate (1.00 g, 4.11 mmol) in methylene chloride (20 mL) was cooled to 0° C., and added with the Dess-Martin reagent (2.27 g, 5.34 mmol), and then the mixture was stirred at room temperature for 4 hours. The reaction mixture was filtered, and the filtrate was washed with saturated aqueous sodium hydrogencarbonate, and then further washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate (0.874 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-8ada52b783d14dfdac81c0773a41f46c
Source noteuspto-grants-2015_10