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HRID 1736554作成日:2026年10月25日

Dimethyl Sulfate → (1-Methoxyphenylethylidene)malononitrile

https://huagongshe.com/reaction/1736554

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物Sodium hydrideHCID 24758—
反応物(1-Hydroxyphenylethylidene)malononitrileHCID 86747658—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Methoxyphenylethylidene)malononitrileHCID 8674765756.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05541187
出典データセットuspto-grants-1996_07
ORD IDord-a0e78d52e24647ccba31e03c81e9ad57
出典メモuspto-grants-1996_07