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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203702Generated: October 30, 2026

4-Toluenesulfonyl chloride → trans-Tert-butyl 4-fluoro-3-(tosyloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2203702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(3R,4R)-1-Boc-4-fluoro-3-piperidinolHCID 67086934—
SolventPyridineHCID 1049—
Producttrans-Tert-butyl 4-fluoro-3-(tosyloxy)piperidine-1-carboxylateHCID 13172971775%

Reaction Steps

A mixture of trans-tert-butyl 4-fluoro-3-hydroxypiperidine-1-carboxylate (3.10 g, 14.1 mmol) and 4-methylbenzene-1-sulfonyl chloride (5.39 g, 28.3 mmol) in pyridine (20 mL) was stirred at room temperature for 18 hours. The pyridine was removed in vacuo, and the residue was dissolved in ethyl acetate (30 mL), washed with brine, dried (sodium sulfate) and concentrated in vacuo. The residue obtained was purified by flash chromatography on silica gel (hexane:ethyl acetate 2:1) to give trans-tert-butyl 4-fluoro-3-(tosyloxy)piperidine-1-carboxylate (3.95 g, 75%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-9aa3200fedca4796bdae4a1b9f8c6dea
Source noteuspto-grants-2016_06