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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021278Generated: October 26, 2026

Methanol → N-Cbz-4,4'-bipiperidine

https://huagongshe.com/reaction/1021278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant4,4'-Bipiperidine dihydrochlorideHCID 12270637—
SolventTolueneHCID 1140—
ProductN-Cbz-4,4'-bipiperidineHCID 1097957640.6%

Reaction Steps

4,4′-Bipiperidine dihydrochloride (2.95 g) was mixed with MeOH (25 ml), and a mixture of benzyl chloroformate (2.2 g) and toluene (5 ml) was added dropwise thereto over 1 hour while keeping the solution neutral by adding a 6 M aqueous NaOH solution at the same time. The reaction mixture was stirred at room temperature for 30 minutes and then concentrated under reduced pressure. CHCl3, and a saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (CHCl3/MeOH) to obtain benzyl 4,4′-bipiperidine-1-carboxylate (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-813829c2e1ed42f6b32da12bf06fa363
Source noteuspto-grants-2014_05