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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168016Generated: October 29, 2026

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

https://huagongshe.com/reaction/2168016

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 numberUS09045475B2
Source datasetuspto-grants-2015_06
ORD IDord-56d92eb8868548be83e7c69ffd25d95a
Source noteuspto-grants-2015_06