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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3670Erstellt: 24. Oktober 2026

Acetic Acid → Acetic acid N-hydroxysuccinimide ester

https://huagongshe.com/de/reaction/3670

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTriethylamineHCID 8471—
EduktDiphenyl chlorophosphateHCID 75654—
EduktN-HydroxysuccinimideHCID 80170—
LösungsmittelEthyl AcetateHCID 8857—
ProduktAcetic acid N-hydroxysuccinimide esterHCID 8446070%

Reaktionsschritte

1.27 g (0.011 mol) of N-hydroxysuccinimide were initially introduced into 10 ml of ethyl acetate, a solution of 3.22 g (0.012 mol) of diphenyl chlorophosphate in 10 ml of ethyl acetate was added and then a solution of 2.53 g (0.025 mol) of triethylamine in 10 ml of ethyl acetate was added dropwise in the course of 10 minutes, the temperature rising to 41° C. A thick, white suspension resulted, which was treated with a solution of 0.6 g (0.01 mol) of acetic acid in 10 ml of ethyl acetate and heated at 45°-55° C. for 16 hours. After ending of the reaction, the solid was filtered off and washed with 2×3 ml of ethyl acetate. The combined filtrates were evaporated in vacuo and the semicrystalline residue which remained was washed by stirring with 20 ml of ethanol for 30 minutes. The white solid thus obtained was filtered off, washed with 2×3 ml of ethanol, sucked dry and then washed by stirring with 10 ml of isopropanol. After filtering off, washing with 2×2 ml of isopropanol and drying in vacuo, 1.1 g (70%) of white acetic acid succinimidyl ester were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05734064
Quelldatensatzuspto-grants-1998_03
ORD IDord-46ef6b3fdcb74f75b3a22e357525e9cd
Quellennotizuspto-grants-1998_03