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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16058Generated: October 26, 2026

Pyridine → 1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidine

https://huagongshe.com/reaction/16058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventChloroformHCID 6212—
Product1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 10642851—

Reaction Steps

A solution of N-Boc-4-piperidinemethanol, 5.0 g (23.2 mmol) in chloroform, 50 mL, was prepared. Toluene sulfonyl chloride, 5.75 g (30.2 mmol), in 5.6 mL of pyridine (69.6 mmol) was added. The solution was stirred under nitrogen allowed to stir for 24 hours. Standard workup and chromatographic purification provided the title compound. Yield 6.0 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737127B2
Source datasetuspto-grants-2010_06
ORD IDord-c7699937794840df9e4605140d7e4fc6
Source noteuspto-grants-2010_06