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Imidazole, 5-(2-chloroethyl)-1-methyl-2-nitro- → 1-ME-2-NO2-5-Vinyl imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole, 5-(2-chloroethyl)-1-methyl-2-nitro- | HCID 90183 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-ME-2-NO2-5-Vinyl imidazole | HCID 93215 | — |
反応手順
To a solution of 18.9 g. of 5-(2-chloroethyl)-1-methyl-2-nitroimidazole (prepared according to the procedure of British Pat. No. 1,222,486) in 2.8 liters of anhydrous benzene cooled to 5°-10° C., 16.8 g. of potassium tert-butoxide is added. Stirring is continued for 2 hours at 5°-10° C. After filtration and concentration to dryness under vacuum at a temperature lower than 50° C., the resulting yellow oily residue is washed three times with 50 ml. of ethyl ether (or light petroleum). The title product is obtained, which is dried under vacuum at 40° C.; yield 12 g. (77.7%). A sample crystallized from ethyl ether melts at 106°-108° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03954789 |
| 出典データセット | uspto-grants-1976_05 |
| ORD ID | ord-1dc4c2dcbd484499bf4d0d95e7d51419 |
| 出典メモ | uspto-grants-1976_05 |