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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465502Generated: October 26, 2026

tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate → Tert-butyl 4-(6-{2-[4-(2-hydroxyethyl)phenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1465502

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—
Reactant[4-(2-Hydroxyethyl)benzyl](triphenyl)phosphonium bromideHCID 86651852—
ProductTert-butyl 4-(6-{2-[4-(2-hydroxyethyl)phenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylateHCID 67030871—

Reaction Steps

By a method similar to Production Example 108, step 4, [4-(2-hydroxyethyl)benzyl](triphenyl)phosphonium bromide (2.866 g, 6.004 mmol) and tert-butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate (1.458 g, 5.003 mmol) were condensed to give tert-butyl 4-(6-{2-[4-(2-hydroxyethyl)phenyl]vinyl}pyridin-3-yl)piperazine-1-carboxylate (5.684 g, quantitatively) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-fe63024ada0b4642be902139a1423100
Source noteuspto-grants-2015_04