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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574832Generated: October 30, 2026

Triethylamine → Tert-butyl (1-(methylsulfonyl)piperidin-3-yl)methylcarbamate

https://huagongshe.com/reaction/574832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-[(piperidin-3-yl)methyl]carbamateHCID 2756030—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (1-(methylsulfonyl)piperidin-3-yl)methylcarbamateHCID 47411127—

Reaction Steps

tert-Butyl piperidin-3-ylmethylcarbamate (500 mg) was dissolved in anhydrous dichloromethane (10 mL), and methanesulfonyl chloride (0.181 mL) was added followed by the addition of triethylamine (1.3 mL). The reaction mixture was stirred at room temperature overnight. The organic solvent was removed under vacuum. The residue was purified with flash column chromatography on silica gel eluting with 0-70% ethyl acetate in hexane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034875B2
Source datasetuspto-grants-2015_05
ORD IDord-6afd9f6c1aa74cc39086dcc516739c0e
Source noteuspto-grants-2015_05