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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835744Generated: October 26, 2026

Acetic Anhydride → 2-nitroethyl Acetate

https://huagongshe.com/reaction/1835744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-NitroethanolHCID 12252—
ReactantSodium AcetateHCID 517045—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product2-nitroethyl AcetateHCID 11815399366%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774126B2
Source datasetuspto-grants-2004_08
ORD IDord-5b68caae2ea54655956e28e44dae174d
Source noteuspto-grants-2004_08