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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1736554Erstellt: 24. Oktober 2026

Dimethyl Sulfate → (1-Methoxyphenylethylidene)malononitrile

https://huagongshe.com/de/reaction/1736554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktSodium hydrideHCID 24758—
Edukt(1-Hydroxyphenylethylidene)malononitrileHCID 86747658—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(1-Methoxyphenylethylidene)malononitrileHCID 8674765756,2%

Reaktionsschritte

To a suspension of 60% NaH/mineral oil dispersion (2.9 g, 74.7 mmol) in THF (50 ml) was added dropwise (1-hydroxyphenylethylidene)malononitrile (13.8 g, 74.7 mmol) in THF (75 ml) over 25 minutes, followed by dimethylsulfate (7.1 ml, 74.7 mmol) in THF (50 ml) over 20 minutes. The reaction mixture was stirred at room temperature for 30 minutes, then at reflux for 4 hours. 0.5 equivalents of 60% sodium hydride and dimethylsulfate were added and the reaction mixture was stirred at room temperature for 24 hours. The solvent was removed in vacuo, the residue was partitioned between ether and water, the organic layer was separated and the aqueous layer was extracted with ether (3×150 ml). The combined organic layers were dried over anhydrous MgSO4 and solvent was removed in vacuo. The residue was purified by column chromatography on silica eluting with ethyl acetate/hexanes (1/1) to afford 8.4 g (56%) of (1-methoxyphenylethylidene)malononitrile as an amber liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05541187
Quelldatensatzuspto-grants-1996_07
ORD IDord-a0e78d52e24647ccba31e03c81e9ad57
Quellennotizuspto-grants-1996_07