Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403611Generated: November 2, 2026

Bromine → Tert-butyl 4-(5-bromo-3-formylpyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2403611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactanttert-Butyl 4-(3-formylpyridin-2-yl)piperazine-1-carboxylateHCID 24741846—
SolventAcetic AcidHCID 176—
ProductTert-butyl 4-(5-bromo-3-formylpyridin-2-yl)piperazine-1-carboxylateHCID 8666797385.9%

Reaction Steps

tert-Butyl 4-(3-formylpyridin-2-yl)piperazine-1-carboxylate (1.88 g) was dissolved in acetic acid (20 ml), and bromine (1.03 g) was added dropwise thereto, followed by stirring at room temperature for 30 minutes. The solvent was evaporated under reduced pressure. The obtained residue was subjected to liquid separation by the addition of CHCl3 and a 1 M aqueous NaOH solution. The organic layer was dried over MgSO4 and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain tert-butyl 4-(5-bromo-3-formylpyridin-2-yl)piperazine-1-carboxylate (2.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-a7c00c3c7fd14f74b1487e90acee8a11
Source noteuspto-grants-2014_08