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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110293Generated: October 25, 2026

Pyridine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine

https://huagongshe.com/reaction/2110293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
SolventDichloromethaneHCID 6344—
ProductN-BOC-3(R)-methylsulfonyloxymethyl-piperidineHCID 10108453—

Reaction Steps

To a stirred solution of N-BOC-3-piperidinemethanol (0.50 g, 0.002 mmole) in DCM (10 mL) was added dropwise pyridine (2.42 mL, 0.03 mmole) followed by the addition of methanesulfonyl chloride (0.774 mL, 0.01 mmole). The reaction mixture continued stirring at RT overnight. The reaction mixture was quenched with water. The aqueous layer was extracted with EtOAc (3×5 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield a crude oil, 68, which was used in the next step without further purification. LRMS: 193 (M+-BOC group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517892B2
Source datasetuspto-grants-2009_04
ORD IDord-afeda98d3cfb400ca8ce872c3c6052a6
Source noteuspto-grants-2009_04