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2-Pentanamine → N-(1-methylbutyl)-4-(methylsulfonyl)-2,6-dinitro-m-toluidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Pentanamine | HCID 12246 | — |
| 反応物 | 3-Chloro-6-(methylsulfonyl)-2,4-dinitrotoluene | HCID 23335973 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | N-(1-methylbutyl)-4-(methylsulfonyl)-2,6-dinitro-m-toluidine | HCID 23335968 | — |
反応手順
A mixture of 3-chloro-6-(methylsulfonyl)-2,4-di-nitrotoluene (10.0 g., 0.034 mole) and 2-aminopentane (6.1 g. 0.07 mole) is refluxed in benzene (75 ml.) for 4 hours. After standing overnight, the mixture is successively washed with dilute hydrochloric acid, water, a 5% aqueous potassium carbonate solution and finally water. The mixture is then dried over magnesium sulfate. Removal of the magnesium sulfate and solvent leaves the desired product as a yellow oil which readily crystallized on cooling. The crude product is recrystallized from ethanol to give 9.5 grams with m.p. 85°-88° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04227913 |
| 出典データセット | uspto-grants-1980_10 |
| ORD ID | ord-894ae7259c644d92a7d8c2883be4ed37 |
| 出典メモ | uspto-grants-1980_10 |