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Hydrochloric Acid → 3-Cyano-2-oxo-8-chromenyloxyacetic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Tetrahydrothiophene | HCID 1127 | — |
| 反応物 | Bromhydrol | HCID 166749 | — |
| 反応物 | 3-Cyano-2-oxo-8-chromenyloxyacetic acid methyl ester | HCID 70353493 | — |
| 溶媒 | Methyl Chloride | HCID 6327 | — |
| 生成物 | 3-Cyano-2-oxo-8-chromenyloxyacetic acid | HCID 70353935 | — |
反応手順
Ten ml of tetrahydrothiophene was cooled with ice, to which 13.4 g of pulverized anhydrous aluminium bromide was gradually added. After stirring for 5 minutes, a temperature was brought to room temperature and then a solution of 2.6 g of 3-cyano-2-oxo-8-chromenyloxyacetic acid methyl ester dissolved in 30 ml of methyl chloride was gradually added. After stirring for 2 hours, the reaction mixture was poured into a mixture of 20 ml of concentrated hydrochloric acid and 200 ml of ice water and a precipitate was filtered, which was recrystallized to give a desired compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04731375 |
| 出典データセット | uspto-grants-1988_03 |
| ORD ID | ord-057f1541b9894369866bc9da13bbcf5d |
| 出典メモ | uspto-grants-1988_03 |