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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887019Generated: October 30, 2026

Toluene → N-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/887019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant4-HydroxyphenylacetoneHCID 7019274—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-butoxycarbonyl)piperidineHCID 701030486.4%

Reaction Steps

A solution of triphenylphosphine (18.5 g, 70.6 mmol) and 40% DEAD in toluene (12.3 g, 70.6 mmol) in 125.0 mL of tetrahydrofuran was cooled to 0° C. under N2 as a solution of 1-(4-hydroxy-phenyl)-propan-2-one (6.54 g, 43.6 mmol) and 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (10.7 g, 53.2 mmol) in 125.0 mL of tetrahydrofuran was added dropwise via addition funnel. After stirred at rt overnight, the solvent was evaporated. The residue was stirred in hexane/EtOAc, the solid formed was filtered. The hexane/EtOAC solution was concentrated and purified by ISCO graduate chromatography (hexane-20% EtOAc in hexane) to give 4-[4-2-oxo-propyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester (8.52 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247414B2
Source datasetuspto-grants-2012_08
ORD IDord-b1634dcbb78b4acda77e6c42de5e752a
Source noteuspto-grants-2012_08