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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2374711Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-[2-(2-Hydroxy-4-nitrobenzoylamino)benzoylamino]butanoic acid

https://huagongshe.com/reaction/2374711

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktChlorotrimethylsilaneHCID 6397—
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
Edukt2-Hydroxy-4-nitrobenzoyl chlorideHCID 12924720—
Edukt4-(2-Aminobenzamido)butanoic acidHCID 13442375—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[2-(2-Hydroxy-4-nitrobenzoylamino)benzoylamino]butanoic acidHCID 23118550—

Reaktionsschritte

To a suspension of 1.00 g (4.50 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 20 ml of dry methylene chloride, add 4.50 g (38.50 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 0.58 g (5.70 mmol) of triethylamine and a solution of 0.77 g (38.50 mmol) of 2-hydroxy-4-nitrobenzoyl chloride dissolved in 10 ml of dry methylene chloride. Allow the reaction to stir for 30 minutes in an ice bath and 24 hours at room temperature. Eliminate the solvent at low pressure, add 30 ml of 10% NaOH to the crude product and continue stirring the mixture until the oil has completely disappeared. Immediately acidify with concentrated HCl, filter the resulting solid and wash several times with water and with ether. Purify the reaction product by recrystallization (EtOH/H2O). This yields 0.50 g (34%) of 4-[2-(2-hydroxy-4-nitro-benzoylamino)benzoylamino]butanoic acid as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07462735B2
Quelldatensatzuspto-grants-2008_12
ORD IDord-df066ac291184abba40f58bf84858170
Quellennotizuspto-grants-2008_12