참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | alpha-(p-Tolylthio)(m-phenoxyphenyl)-acetonitrile | HCID 12945139 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrile | HCID 13023169 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04340740 |
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| 출처 데이터셋 | uspto-grants-1982_07 |
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| ORD ID | ord-41e3db438f8244859a3e784bcced1f33 |
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| 출처 메모 | uspto-grants-1982_07 |
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