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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891713Generated: October 28, 2026

Sodium Azide → 4-Azido-1-(p-nitrobenzyloxycarbonyl)piperidine

https://huagongshe.com/reaction/891713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant4-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)piperidineHCID 22242766—
SolventDimethylformamideHCID 6228—
Product4-Azido-1-(p-nitrobenzyloxycarbonyl)piperidineHCID 22242714100%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)piperidine (3.31 g, 9.24 mmol) (obtained as described in Reference Example 51(2)) in dimethylformamide (100 ml) was added sodium azide (660 mg, 10.2 mmol), and the mixture was stirred in an oil bath (100° C.) for 3 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (3:1→1:1) as the eluant to afford 4-azido-1-(p-nitrobenzyloxycarbonyl)piperidine (2.81 g, yield 100%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-ee2f0db8f5394a69917cf025070d9a0c
Source noteuspto-grants-2006_02