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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49769Generated: October 26, 2026

Pyridine → tert-Butyl (1-acetylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/49769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDichloromethaneHCID 6344—
Producttert-Butyl (1-acetylpiperidin-4-yl)carbamateHCID 22741830—

Reaction Steps

To a suspension of O-tert-butyl N-(piperidin-4-yl)carbamate (4.0 g) in dichloromethane (40 ml) were added pyridine (1.94 ml), dichloromethane (40 ml), acetic anhydride (20.8 ml) and then N,N-dimethylaminopyridine (0.1 g) at ambient temperature. After stirring for 3 hours, the mixture was washed with 0.1N hydrochloric acid, water, and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. After rinse with diisopropyl ether, O-tert-butyl N-(1-acetylpiperidin-4-yl)carbamate (4.01 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-b12d37f21ea84368a39ce8b587735be1
Source noteuspto-grants-2004_03