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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634201Generated: October 30, 2026

N-bromobutanimide → 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine

https://huagongshe.com/reaction/1634201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylateHCID 10778540—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidineHCID 1068397087.8%

Reaction Steps

NBS (1.4 g) was added to a solution of 1-tert-butoxycarbonyl-1,2,3,6-tetrahydro-4-(trimethylsilyloxy)pyridine (2 g) in acetonitrile and the mixture was stirred at room temperature for 30 minutes. The solution was diluted with ethyl acetate(50 ml) and washed with water (50 ml), sodium bicarbonate solution (50 ml) and brine (50 ml), dried (MgSO4) and evaporated to give the title compound as a colourless solid (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506773B2
Source datasetuspto-grants-2003_01
ORD IDord-9e50011067924b0aa3bd679630e21393
Source noteuspto-grants-2003_01