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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120076Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 4-(4-formylphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2120076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventPyridineHCID 1049—
ProductTert-butyl 4-(4-formylphenyl)piperazine-1-carboxylateHCID 2795509—

Reaction Steps

1-(t-Butoxycarbonyl)piperazine (1.86 g, 10 mmol), p-fluorobenzaldehyde 27 (1.24 g, 10 mmol), and K2CO3 (1.74 g, 11 mmol) in dry pyridine (10 mL) are stirred at reflux under a nitrogen atmosphere for 24 h. Most of the solvent is removed under vacuum and the residue is partitioned between EtOAc (150 mL) and water (100 mL). The aqueous layer is washed with EtOAc (2×50 mL) and the combined organic layers are sequentially washed with 3% aq. citric acid (2×100 mL), water (100 mL), brine (100 mL), and dried (MgSO4). The solvent is removed under vacuum and the residue washed with hexanes and dried under vacuum. The product can be used as such, or further purified by silica gel column chromatography (dichloromethane-MeOH gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689769B2
Source datasetuspto-grants-2004_02
ORD IDord-663a39e12a7742f5b80085dff4892ff7
Source noteuspto-grants-2004_02