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Ethanol → 5-Cyanomethylbenz-2,1,3-thiadiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | 5-(Bromomethyl)-2,1,3-benzothiadiazole | HCID 591004 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-Cyanomethylbenz-2,1,3-thiadiazole | HCID 69522445 | 53.3% |
反応手順
A mixture of 5-bromomethyl-benzo[1,2,5]thiadiazole [RN65858-50-6](7.0 g, 30 mmol), ethanol (50 ml)and a solution of potassium cyanide (2.3 g, 36 mmol) in water (25 ml) was stirred at 50° C. for 15 hours. The alcoholic solution was concentrated and the residue suspended in water. The solid was collected by filtration, washed with water and dried in vacuo to give benzo[1,2,5]thiadiazol-5-yl-acetonitrile (2.8 g, 47%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07186730B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-a391e509cf0c4b54be8190b45336aff2 |
| 出典メモ | uspto-grants-2007_03 |