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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113603Generated: October 29, 2026

Sodium Azide → tert-butyl (3S)-3-aminopiperidine-1-carboxylate

https://huagongshe.com/reaction/2113603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactanttert-Butyl (3R)-3-[(methanesulfonyl)oxy]piperidine-1-carboxylateHCID 29939737—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—

Reaction Steps

Sodium azide (7.65 g, 118 mmol) was added to a solution of 1,1-dimethylethyl (3R)-3-[(methylsulfonyl)oxy]-piperidine-1-carboxylate (21.9 g, 78.5 mmol) in dry dimethylformamide (120 mL) and the resultant suspension heated at 70° C. for 48 hours. After cooling to room temperature, the reaction mixture was diluted with water and extracted into ethyl acetate. The organic phase was washed two further times with water, then brine. The organic extracts were dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (10:90 to 50:50), to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432280B2
Source datasetuspto-grants-2008_10
ORD IDord-78e84d22302c4761b6711cd543c23308
Source noteuspto-grants-2008_10