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Benzonitrile → 2-Aminobenzothiazole-6-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzonitrile | HCID 7505 | — |
| 反応物 | 4-Aminobenzonitrile | HCID 13396 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Potassium thiocyanate | HCID 516872 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Aminobenzothiazole-6-carbonitrile | HCID 4327139 | — |
反応手順
4-Aminobenzonitrile is dissolved in acetic acid (or a weak protic acid) and the solution is cooled to about 16–30° C., preferably 16–18° C. Potassium thiocyanate is added and the flask is then equipped with an addition funnel. The addition funnel is charged with bromine and acetic acid. This dark solution is then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 12–20 hours, preferrably about 16 hours. The slurry is then drowned into water and filtered. The presscake is washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake is washed well with water to obtain the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091227B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-6eca5615015f4ce68df2769bea908bce |
| 出典メモ | uspto-grants-2006_08 |