関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Ethanone, 2-(acetyloxy)-1-phenyl- | HCID 222851 | — |
| 反応物 | alpha-(Benzothiazol-2-yl)-acetate | HCID 7128533 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(Benzothiazol-2-yl)-4-Phenyl-2-(5H) Furanone | HCID 54181341 | — |
反応手順
A solution of 2-acetoxyacetophenone (from Example 1) (8.9 g, 0.05M) and α-(benzothiazol-2-yl)-acetate (from Example 3) dissolved in methanol (40 mL) by stirring at room temperature was treated at room temperature with a solution prepared by dissolving sodium hydroxide pellets (2.5 g) in methanol (30 mL) by stirring. A slight exothermic reaction was observed. After being stirred at about room temperature for about 1.0 hour, the reaction mixture was acidified to a pH of about 4 by the dropwise addition of concentrated HCl. The product which was a dark brown colored semi-crystalline mass was washed by decantation and dried in air (yield--12.0 g (81.9% of the theoretical yield). Mass spectrometry indicated that the product largely consisted of the following desired compound: ##STR16##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05274072 |
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| 出典データセット | uspto-grants-1993_12 |
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| ORD ID | ord-6a524c00b0354527b91f0643f335c8bc |
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| 出典メモ | uspto-grants-1993_12 |
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