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Acetic Acid → p-Toluenesulfonic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | dibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate | HCID 20185706 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 生成物 | 3-(Hydroxyamino)propylphosphonic acid | HCID 342170 | — |
反応手順
A mixture of dibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate (28.4 g), 6N hydrochloric acid (280 ml) and acetic acid (280 ml) was refluxed with stirring for 20 hours. The resultant mixture was concentrated under reduced pressure to give a residue, and then water was added thereto. The mixture was treated with an activated charcoal, whereafter the mixture was concentrated under reduced pressure to give an oily residue. The oily residue was washed with ether and dried under reduced pressure. The solid was washed with acetonitrile and ethyl ether to give p-toluenesulfonic acid salt of 3-(N-hydroxyamino)propylphosphonic acid (12.4 g) in the form of crystals. M.P.: 129°-135° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04693742 |
| 出典データセット | uspto-grants-1987_09 |
| ORD ID | ord-2354d61a2f484c5b8d76ed12e7f6b6d0 |
| 出典メモ | uspto-grants-1987_09 |