참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isoamyl Nitrite | HCID 8053 | — |
| 반응물 | m-Phenoxybenzyl cyanide | HCID 40075 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrile | HCID 85308279 | 45% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06251926B1 |
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| 출처 데이터셋 | uspto-grants-2001_06 |
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| ORD ID | ord-4315ba764d5148efaf6776f8b73e386d |
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| 출처 메모 | uspto-grants-2001_06 |
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