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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 536587Erstellt: 24. Oktober 2026

4-Nitrobenzoic Acid → HCID 66848190, Verbindung

https://huagongshe.com/de/reaction/536587

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrobenzoic AcidHCID 6108—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukttert-butyl (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 11078078—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 66848190HCID 66848190—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(2S,4R)-4-(Tert-butyl-dimethyl-silanyloxy)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (intermediate 53, 51.4 g, 155 mmol) dissolved in 500 ml of dichloromethane was cooled to 0° C., then p-nitrobenzoic acid (28.5 g, 171 mmol), N,N′-dicyclohexylcarbodiimide (35.2 g, 171 mmol) and 4-dimethylaminopyridine (1.90 g, 1.60 mmol) were added. The mixture was maintained under stirring at room temperature for 18 hours, then filtrated; the filtrate was concentrated to obtain crude that was purified by silica gel chromatography (petroleum ether/ethyl acetate from 15/1 to 10/1). (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(4-nitro-benzoyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester was obtained as white solid (70 g, yield: 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859608B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-aedafc3454554af78953524a7ae56442
Quellennotizuspto-grants-2014_10