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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021289Generated: October 31, 2026

2,6-Di-tert-butylpyridine → HCID 86686240, compound

https://huagongshe.com/reaction/1021289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butylpyridineHCID 68510—
ReactantBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
ReactantTert-butyl 4-(2-iodoethyl)piperidine-1-carboxylateHCID 9974426—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
SolventDichloromethaneHCID 6344—
ProductHCID 86686240HCID 8668624044.8%

Reaction Steps

tert-Butyl 4-(2-iodoethyl)piperidine-1-carboxylate (6.75 g) was mixed with dichloromethane (90 ml), and benzyl 4-hydroxypiperidine-1-carboxylate (4.0 g), silver trifluoromethane sulfonate (10.3 g), and 2,6-di-tert-butylpyridine (12 ml) was added thereto, followed by stirring at room temperature overnight. The reaction mixture was filtered using Celite as a filtration adjuvant, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain tert-butyl 4-[2-({1-[(benzyloxy)carbonyl]piperidin-4-yl}oxy)ethyl]piperidine-1-carboxylate (3.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-d4aa45a62ddf4affae13744d6e3f6634
Source noteuspto-grants-2014_05