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Sodium Hydroxide → 2-[N-(2,4,6-trifluorophenyl)sulfamoyl] acetic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-[N-(2,4,6-trifluorophenyl)sulfamoyl]-acetic acid methyl ester | HCID 15057600 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 2-[N-(2,4,6-trifluorophenyl)sulfamoyl] acetic acid | HCID 15057601 | — |
反応手順
1.37 g (4.8 mmol) of 2-[N-(2,4,6-trifluorophenyl)sulfamoyl]-acetic acid methyl ester is dissolved in 15 ml of dioxane, 7.5 ml of 2N sodium hydroxide solution is added and it is stirred for one hour at room temperature. The solution is then evaporated to dryness, the residue is dissolved in water, the solution is acidified with 2N hydrochloric acid and extracted twice with ethyl acetate. The ethyl acetate extract is dried on magnesium sulfate, filtered and evaporated to dryness. The residue is crystallized from diethyl ether. 1.12 g (4.16 mmol)=86.68% of the theoretical yield is obtained. Melting point 126-127° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05130119 |
| 出典データセット | uspto-grants-1992_07 |
| ORD ID | ord-7068af3026e04935ba61ca13c7ac8a53 |
| 出典メモ | uspto-grants-1992_07 |