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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827240Generated: October 28, 2026

Sodium Azide → Benzyl 4-(azidomethyl)-4-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/1827240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantBenzyl 4-fluoro-4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylateHCID 22135556—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(azidomethyl)-4-fluoropiperidine-1-carboxylateHCID 2213565280%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of benzyl 4-fluoro-4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate (1.3 g, 3.7 mmol) in DMF (10 mL) at RT was added NaN3 (2.4 g, 37.0 mmol). The reaction mixture was heated to 110° C. and stirred for 60 h, cooled and partitioned between EtOAc and H2O. The organic layer was dried over Na2SO4, filtered, concentrated and purified on silica gel (10:1 to 1:2 hexanes:EtOAc) to give benzyl 4-(azidomethyl)-4-fluoropiperidine-1-carboxylate. (0.86 g, 80% yield). M.S. (M+1): 293

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-eefe7973dc804bcd8b26b27a808afb53
Source noteuspto-grants-2006_05