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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759421생성일: 2026년 10월 24일

Methyl iodide → alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrile

https://huagongshe.com/reaction/1759421

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium MethoxideHCID 10942334—
반응물alpha-(p-Tolylthio)(m-phenoxyphenyl)-acetonitrileHCID 12945139—
용매MethanolHCID 887—
생성물alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrileHCID 1302316986%

반응 단계

1.245 g of alpha-(p-tolylthio)(m-phenoxyphenyl)-acetonitrile was dissolved in 5 ml of anhydrous methanol, and a 2.2 M methanol solution of sodium methoxide was added at room temperature in an atmosphere of argon. The mixture was stirred, and 0.35 ml of methyl iodide was added dropwise. The mixture was further stirred for 30 minutes at room temperature. Then, an aqueous solution of ammonium chloride (3 g/20 ml) was added, and the mixture was extracted with 20 ml of ether three times. The extract was washed with 30 ml of water three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The oily residue was purified by column chromatography (silica gel; hexane and methylene chloride) to afford 1.125 g (yield 86%) of alpha-(p-tolylthio)-alpha-(m-phenoxyphenyl)propionitrile as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04340740
출처 데이터셋uspto-grants-1982_07
ORD IDord-41e3db438f8244859a3e784bcced1f33
출처 메모uspto-grants-1982_07