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HRID 6111Erstellt: 23. Oktober 2026

3,5-Di-tert-butyl-4-hydroxybenzoic acid → 4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridine

https://huagongshe.com/de/reaction/6111

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
EduktN-HydroxysuccinimideHCID 80170—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt4-(3-Aminopropylthio)pyridineHCID 15227695—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridineHCID 1907915927,3%

Reaktionsschritte

To a solution of 1.49 g (5.94 mmol) of 3,5-di-t-butyl-4-hydroxybenzoic acid and 889 mg (7.73 mmol) of N-hydroxysuccinimide in 60 ml of methylene chloride was added 1.38 g (7.13 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. Further 1.00 g (5.94 mmol) of 4-(3-aminopropylthio)pyridine was added and the mixture was stirred at rcom temperature for 8 hours. The reaction mixture was washed with water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 650 mg of the desired compound (27.3%, colorless powder), mp: 203.0°-204.0° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246948
Quelldatensatzuspto-grants-1993_09
ORD IDord-2c8dc63242cc44cab385e6bb518c6cff
Quellennotizuspto-grants-1993_09