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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253249Generated: October 26, 2026

Ethyl Acetate → 2-(3,4-Bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrile

https://huagongshe.com/reaction/253249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant(3,4-Bis{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrileHCID 66888874—
SolventTetrahydrofuranHCID 8028—
Product2-(3,4-Bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrileHCID 6689091686.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of (3,4-bis{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile (0.59 g, 2.2 mmol), and sodium hydride (40% oil dispersion, 270 mg, 6.7 mmol) in tetrahydrofuran (10 mL), was added ethyl acetate (1.1 mL, 11.1 mmol), and the resulting mixture was stirred at 60° C. for 1.5 hours. Then it was cooled to room temperature, and poured into a mixture of ice-water (50 mL). This aqueous mixture was washed with dichloromethane (3×20 mL) then acidified to pH of 2. The acidified mixture was extracted with ethyl acetate (3×30 mL). The combined extract was washed with saturated sodium bicarbonate solution, brine, dried over sodium sulfate, filtered and concentrated to give 2-(3,4-bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxobutanenitrile (0.57 g, 1.9 mmol, 86% yield), MS (EI) for C16H21NO5: 308 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-a6c19d6caeb249298a51aeef550cfa9d
Source noteuspto-grants-2011_01