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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042564Generated: November 1, 2026

Toluene → N-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/2042564

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 numberUS08586588B2
Source datasetuspto-grants-2013_11
ORD IDord-48b3d4309f0e4938a52022455a1267e0
Source noteuspto-grants-2013_11