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Ethyl Bromide → 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Bromide | HCID 6332 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 1-(4-Nitrophenyl)pyrimidine-2,4-dione | HCID 11276338 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione | HCID 15125479 | 65.6% |
反応手順
A mixture of 3 parts of 1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione, 1,4 parts of potassium hydroxide and 67.5 parts of N,N-dimethylacetamide was stirred for 1 hour at room temperature under nitrogen atmosphere. 1.52 Parts of bromoethane were added and stirring was continued overnight at room temperature. The reaction mixture was poured into 100 parts of ice water. The product was filtered off and stirred in methanol. The product was filtered off and dried in vacuo at 60° C., yielding 2.4 parts (65.6%) of 3-ethyl-1-(4-nitro-phenyl)-2,4(1H,3H)-pyrimidinedione; mp. 182.5° C. (int. 24).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04931444 |
| 出典データセット | uspto-grants-1990_06 |
| ORD ID | ord-d072a9a384e947f2a9bfee02dda21a87 |
| 出典メモ | uspto-grants-1990_06 |