HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928639Generated: October 25, 2026
Acetic Acid → 2-(1-(Trimethylsilyl)ethylidene) malononitrile
https://huagongshe.com/reaction/928639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Acetyltrimethylsilane | HCID 638116 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(1-(Trimethylsilyl)ethylidene) malononitrile | HCID 86691500 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09290526B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-236312ca11b944568be2aebed09b12c4 |
|---|
| Source note | uspto-grants-2016_03 |
|---|