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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715913Generated: October 28, 2026

Water → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/715913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—

Reaction Steps

To a solution of tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate (2.5 g) in dichloromethane (40 ml), triethylamine (2.8 ml) and methanesulfonyl chloride (1.2 ml) were added under ice cooling, and the mixture was stirred at room temperature for 3 hours. Water was added to the reaction solution to separate two layers. Then, the aqueous layer was subjected to extraction with chloroform. The organic layers were combined, washed with saturated saline and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane-ethyl acetate) to obtain the title compound (2.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187489B2
Source datasetuspto-grants-2015_11
ORD IDord-b30dd5ad0f6b4a178014d6817d7a5514
Source noteuspto-grants-2015_11