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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2100665Erstellt: 25. Oktober 2026

Hydrochloric Acid → tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2100665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktTert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 67030211—
Produkttert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—

Reaktionsschritte

To a solution of tert-butyl 4-(6-cyano-pyridin-3-yl)-piperazine-1-carboxylate (2.15 mmol) in THF (20 mL) is added a solution of DIBAL-H in THF (1.0 M, 13 mmol) dropwise and the reaction mixture is stirred at room temperature for 15 minutes. After it is cooled to 0° C., the reaction mixture is mixed with a solution of aqueous HCl (2 N, 5 mL) after which the reaction mixture is partitioned between saturated Na2CO3 solution and EtOAc. The aqueous phase is extracted with EtOAc. The combined organic extracts are washed with saturated aqueous NaCl and dried over Na2SO4. After concentration, the residue is purified by silica gel chromatography (3:7 hexanes/EtOAc) to give tert-butyl 4-(6-formyl-pyridin-3-yl)-piperazine-1-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07572811B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-07288dd9e14e47ea90d15f87eb67aeb8
Quellennotizuspto-grants-2009_08