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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896511Generated: October 30, 2026

Sodium Azide → tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/896511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactanttert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylateHCID 22647269—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-(azidomethyl)piperidine-1-carboxylateHCID 2264738098.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 3-methanesulfonyloxymethylpiperidine-1-carboxylic acid tert-butyl ester (19.11 g, 65.1 mmol) in N,N-dimethylformamide (125 mL) was treated with sodium azide (12.70 g, 195 mmol) and the mixture was stirred at 50° C. for 22 hours. The mixture was cooled and filtered, and the filtrate was concentrated under vacuum. The residue was dissolved in ethyl acetate, washed with water, dried over sodium sulfate, and concentrated under vacuum to provide a colorless liquid (15.34 g, 98%) which was used without further purification. 1H NMR (300 MHz, CDCl3) δ3.95 (bd, J=12 Hz, 1H), 3.86 (dt, J=13, 4 Hz, 1H), 3.22 (d, J=7 Hz, 2H), 2.87 (ddd, J=14, 11, 3 Hz, 1H), 2.68 (m, 1H), 1.9-1.6 (3H), 1.49 (m, 1H), 1.47 (s, 9H), 1.26 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919356B2
Source datasetuspto-grants-2005_07
ORD IDord-43f9ce1bc4a74c4cbd651f79cf06b34c
Source noteuspto-grants-2005_07