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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13554Erstellt: 23. Oktober 2026

4-Formylbenzoic acid → Tert-butyl 4-(4-formylbenzoyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/13554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Formylbenzoic acidHCID 12088—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(4-formylbenzoyl)piperazine-1-carboxylateHCID 59218188—

Reaktionsschritte

A suspension of 4-carboxybenzaldehyde (3.10 g) in CH2Cl2 was treated sequentially with piperazine-1-carboxylic acid tert-butyl ester (3.6 g), EDCl (3.86 g), HOBt (2.68 g), and 4-dimethylaminopyridine (˜0.020 g). After 18 h, the mixture was extracted with 1 N NaOH and then with 1 N HCl. The organic layer was dried (Na2SO4) and concentrated to yield the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728129B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9f2266dfe35b4b34a5f82d1e7a0771b8
Quellennotizuspto-grants-2010_06