関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isoamyl Nitrite | HCID 8053 | — |
| 反応物 | m-Phenoxybenzyl cyanide | HCID 40075 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrile | HCID 85308279 | 45% |
反応手順
To a solution of sodium ethoxide prepared from sodium (1.09 g) and ethanol (20 ml), a solution of 3-phenoxyphenylacetonitrile (8.30 g) in ethanol (15 ml) was added dropwise at 0° C., and then isoamyl nitrite (7.99 ml) was added dropwise. After stirring for 15 hours at room temperature, diethyl ether was added and the mixture was washed sequentially with 1N HCl, aqueous sodium bicarbonate and then saturated aqueous sodium chloride. The diethyl ether layer was dried (MgSO4), concentrated, and the residue was subjected to column chromatography on silica gel. The crystals obtained from a fraction eluted with ethyl acetate-hexane (1:4, v/v) were recrystallized with ethyl acetate-hexane to obtain 2-hydroxyimino-2-(3-phenoxyphenyl)acetonitrile (4.25 g, yield: 45%) as pale-yellow crystals. A mixture of the E- form and the Z- form. m.p. 124-125° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06495581B1 |
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| 出典データセット | uspto-grants-2002_12 |
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| ORD ID | ord-20613cfbb7604198840da3b3eac470b1 |
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| 出典メモ | uspto-grants-2002_12 |
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