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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69982Generated: October 28, 2026

Triethylamine → (3S,5R)-benzyl 3-azido-5-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/69982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 59455657HCID 59455657—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(3S,5R)-benzyl 3-azido-5-fluoropiperidine-1-carboxylateHCID 5945572990%

Reaction Steps

To a solution of (3R,5R)-benzyl 3-fluoro-5-hydroxypiperidine-1-carboxylate (1 eq) in 14 mL of dichloromethane was added triethyl amine (3 eq) and methanesulfonyl chloride (1.5 eq) at 0° C. The reaction mixture was allowed to stir at room temperature for 1.5 hours. The crude mixture was diluted with 120 mL of diethyl ether, washed with sat. aq. sodium bicarbonate, brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was dissolved in 16 mL of NMP. Sodium azide (3.0 eq) was added and the resulting suspension was stirred at 80° C. overnight. The reaction mixture was diluted with 200 mL of EtOAc and 100 mL of hexanes, washed with water, brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (EtOAc: hexanes=1:3) to give the titled compound (90%). LC/MS (m/z): 251.1 (MH+-28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-4272bcda668c4ef4835bdc7634b32fd1
Source noteuspto-grants-2014_09