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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494014Generated: October 30, 2026

4,4'-Bipiperidine dihydrochloride → 4,4'-Bipiperidine, 1-boc protected

https://huagongshe.com/reaction/494014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-Bipiperidine dihydrochlorideHCID 12270637—
ReactantTert-butyldicarbonateHCID 22064466—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product4,4'-Bipiperidine, 1-boc protectedHCID 1174759972%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution is prepared of 41 g (0.17 M) of 4,4′-bipiperidine dihydrochloride in 250 ml of ethanol and 250 ml of 2N sodium hydroxide. A solution of 18.5 g (0.085 M) of t-butyl dicarbonate in 100 ml of ethanol are added slowly, at 0° C. The reaction mixture is agitated for 1 hour at 10° C. and the ethanol is then removed by an evaporator, under reduced pressure. The residual aqueous phase is saturated with sodium chloride and extracted with ethyl acetate. The organic phase obtained is dried over magnesium sulphate and concentrated under reduced pressure. The crude product is purified by silica gel chromatography in eluting with the aid of a dichloromehane/methanol/aqueous ammonia mixture (8/2/0.4; v/v/v). 16.5 g of the compound sought after are thus obtained as a white solid (yield=72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538111B2
Source datasetuspto-grants-2009_05
ORD IDord-c75086f5b7984dd5a4371536ebd168c0
Source noteuspto-grants-2009_05