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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410261Generated: October 25, 2026

Acetic Acid → 2-(1-(Trimethylsilyl)ethylidene) malononitrile

https://huagongshe.com/reaction/2410261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMalononitrileHCID 8010—
ReactantAmmonium AcetateHCID 517165—
ReactantAcetyltrimethylsilaneHCID 638116—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product2-(1-(Trimethylsilyl)ethylidene) malononitrileHCID 8669150080%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a mixture of acetyltrimethylsilane (1.0 g, 8.6 mmol), malononitrile (625 mg, 9.46 mmol) and ammonium acetate (126 mg, 1.64 mmol), acetic acid (394 μL, 6.88 mmol) and benzene (30 mL) were added. The reaction flask was attached to a Dean-Stark trap filled with benzene and the solution was heated to 95° C. for 3 h. The orange reaction mixture was cooled, diluted with EtOAc, washed with saturated aqueous NaHCO3 and brine, dried over anhydrous MgSO4, and concentrated. The residue was purified by column chromatography on silica gel (using a solvent gradient from 1% to 30% EtOAc in hexanes) to give 2-(1-(trimethylsilyl)ethylidene) malononitrile as colorless oil (1.13 g, 79.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816082B2
Source datasetuspto-grants-2014_08
ORD IDord-2b503b0e1b0a411fbd1a24a275d5ecc6
Source noteuspto-grants-2014_08