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Ethylenediamine → ({[2,2-Dimethoxy-1-methyl-1-(nitromethyl)ethyl]thio}methyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylenediamine | HCID 3301 | — |
| 反応物 | Nitromethane | HCID 6375 | — |
| 反応物 | Benzyl mercaptan | HCID 7509 | — |
| 反応物 | Pyruvic aldehyde dimethyl acetal | HCID 80650 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | ({[2,2-Dimethoxy-1-methyl-1-(nitromethyl)ethyl]thio}methyl)benzene | HCID 59135973 | 48% |
反応手順
A mixture of 1,1-dimethoxyacetone (5.00 ml), benzylmercaptan (5.50 ml), nitromethane (23 ml), ethylenediamine (3.00 ml) and acetonitrile (15 ml) was stirred at room temperature, and then overnight at 80° C. The reaction mixture was concentrated, and the obtained residue was subjected to silica gel column chromatography to give the title compound (5.81 g, yield 48%) as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:6, volume ratio).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07777047B2 |
| 出典データセット | uspto-grants-2010_08 |
| ORD ID | ord-7b190cda145f45fca56ec4a45b4448ed |
| 出典メモ | uspto-grants-2010_08 |