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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368059Generated: October 31, 2026

Ethanol → tert-butyl [(1S)-1-methyl-2-(piperidin-4-yloxy)ethyl]carbamate

https://huagongshe.com/reaction/2368059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamateHCID 57517478—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
Producttert-butyl [(1S)-1-methyl-2-(piperidin-4-yloxy)ethyl]carbamateHCID 5751747976.3%

Reaction Steps

To a solution of tert-butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate (1.03 g) in acetic acid (10 mL)/ethanol (10 mL) was added platinum oxide (500 mg), and the reaction mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere. The catalyst was filtered off, and the filtrate was concentrated. The obtained residue was dissolved in 0.5 M hydrochloric acid, and the solution was washed with ethyl acetate, basified with potassium carbonate, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give the title compound (805 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-c348968e42ff4034a9b3259e6b2fa7c6
Source noteuspto-grants-2014_04