関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Aniline | HCID 6115 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Ethyl 2-cyano-3-phenylpropanoate | HCID 228103 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 3-Phenylindole-2-carbonitrile | HCID 12412080 | — |
反応手順
A solution of 4.08 g. (0.044 mol) of aniline in 18 ml. of concentrated hydrochloric acid and 50 ml. of water was maintained below 5° while a solution of 3.00 g. (0.043 mol) of sodium nitrite in 10 ml. of water was added. This solution was then added to a mixture of 8.30 g. (0.041 mol) of α-cyanobenzenepropanoic acid ethyl ester, 50 ml. of ethanol, 100 ml. of water, and 18 ml. of 50% potassium hydroxide solution maintained below 0°. After stirring for an additional 20 minutes the reaction was diluted with water and shaken with ether. Some insoluble solid was removed by filtration and the ether layer was concentrated. The residue was heated on the steam bath for 4 hours with 60 ml. of acetic acid and 60 ml. of concentrated hydrochloric acid. The cooled reaction was diluted with water and extracted with dichloromethane. The extracts were dried, filtered over some silica gel and concentrated. Recrystallization of the residue from dichloromethane-hexane gave 3-phenylindole-2-carbonitrile as tan crystals, m.p. 137°-142°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04156016 |
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| 出典データセット | uspto-grants-1979_05 |
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| ORD ID | ord-59cd4715d355409f9aa5e6d3b8845c03 |
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| 出典メモ | uspto-grants-1979_05 |
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