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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384702Generated: October 26, 2026

4-Toluenesulfonyl chloride → Tert-butyl 4-fluoro-4-((tosyloxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/384702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylateHCID 22248400—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-fluoro-4-((tosyloxy)methyl)piperidine-1-carboxylateHCID 5945578480.4%

Reaction Steps

p-Toluenesulfonyl chloride (230 mg, 1.209 mmol) was added portionwise to tert-butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate (188 mg, 0.806 mmol), triethylamine (227 μL, 1.612 mmol), and DMAP (9.85 mg, 0.081 mmol) in dichloromethane (2015 μL) at 0° C. The solution was stirred at room temperature overnight and then partitioned between dichloromethane and water. The organic layer was washed with 0.2M HCl and then dried (MgSO4) and concentrated. The residue was dissolved in dichloromethane and loaded onto a 25+M Biotage silica column. Chromatography, eluting with a gradient of EtOAc in hexanes, gave tert-butyl 4-fluoro-4-(tosyloxymethyl)piperidine-1-carboxylate (251 mg, 0.648 mmol, 80%) as a clear semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367658B2
Source datasetuspto-grants-2013_02
ORD IDord-50706a37e1f74f7da28cb79ba6a8c24d
Source noteuspto-grants-2013_02