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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736554생성일: 2026년 10월 24일

Dimethyl Sulfate → (1-Methoxyphenylethylidene)malononitrile

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

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Sodium hydrideHCID 24758—
반응물(1-Hydroxyphenylethylidene)malononitrileHCID 86747658—
용매TetrahydrofuranHCID 8028—
생성물(1-Methoxyphenylethylidene)malononitrileHCID 8674765756.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05541187
출처 데이터셋uspto-grants-1996_07
ORD IDord-a0e78d52e24647ccba31e03c81e9ad57
출처 메모uspto-grants-1996_07