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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606184Generated: October 31, 2026

Methanesulfonyl chloride → HCID 22248300, compound

https://huagongshe.com/reaction/606184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 4-[(2-aminophenoxy)methyl]piperidine-1-carboxylateHCID 22248383—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 22248300HCID 2224830090%

Reaction Steps

After dissolving 400 mg of 1-(tert-butoxycarbonyl)-4-(2-aminophenoxymethyl)piperidine in 10 ml of tetrahydrofuran, 0.24 ml of triethylamine and 0.12 ml of methanesulfonyl chloride were added and the mixture was stirred overnight at room temperature. Next, 0.24 ml of triethylamine and 0.12 ml of methanesulfonyl chloride were added to the reaction solution and stirring was continued at room temperature for 2 hours. The reaction solution was filtered with silica gel and NH silica gel, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (447 mg, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-a3b976cbc7424ddcaabd67e07e9cbaa7
Source noteuspto-grants-2011_03