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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1267216Erstellt: 26. Oktober 2026

Acetic Anhydride → 2-nitroethyl Acetate

https://huagongshe.com/reaction/1267216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt2-NitroethanolHCID 12252—
EduktSodium AcetateHCID 517045—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-nitroethyl AcetateHCID 11815399366%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

Ex-2a) A mixture of sodium acetate (6.4 g, 78 mmol) and acetic anhydride (30 mL, 330 mmol) was stirred at 0-5° C. To this slurry was added 2-nitroethanol (30 g, 280 mmol) dropwise over a period of approximately 1 hour. After the 2-nitroethanol addition, the orange reaction mixture was stirred at 0-5° C. for an additional hour and then at ambient temperature for approximately 70 min, the exotherm of the reaction increased the temperature to 30° C. and the mixture was cooled with an ice bath to 20° C. The reaction was then stirred at ambient temperature under N2 overnight. The reaction mixture was diluted with ethyl acetate (EtOAc, 40 mL) and saturated brine (80 mL). The layers were separated and the bottom aqueous layer was extracted again with ethyl acetate (25 mL). The combined ethyl acetate layers were washed once with saturated brine (50 mL), dried (MgSO4), filtered and concentrated to afford 38 g of 2-nitroethylacetate as a reddish orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06552052B2
Quelldatensatzuspto-grants-2003_04
ORD IDord-ae428b2a431d43a2869f78dbfd09cb7e
Quellennotizuspto-grants-2003_04