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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593098Generated: October 25, 2026

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

https://huagongshe.com/reaction/1593098

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 numberUS07294637B2
Source datasetuspto-grants-2007_11
ORD IDord-89a7e0ebd0a64870bd0bd14890ed5a87
Source noteuspto-grants-2007_11