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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586388Generated: October 30, 2026

Methanesulfonyl chloride → tert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/586388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylateHCID 22647269—

Reaction Steps

To a solution of 3-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (9.41 g, 0.048 mol) in dichloromethane (200 mL) at room temperature was added iPr2NEt (14.1 g, 0.110 mol), followed by MsCl (5.5 g, 0.048 mol). The reaction mixture was allowed to stir for one hour before concentrating and purifying the resulting residue by silica gel chromatography (1:1 hexane:ethyl acetate). The desired compound was obtained as an oil (11.06 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936614B2
Source datasetuspto-grants-2005_08
ORD IDord-6a9574c2328d40628d6fdf7d1e42f121
Source noteuspto-grants-2005_08