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Hydrochloric Acid → 2-Carbamoyl-7-(3-chloro-2-hydroxypropoxy)benzofuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-Carbamoyl-7-(2,3-epoxypropoxy)benzofuran | HCID 13729403 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-Carbamoyl-7-(3-chloro-2-hydroxypropoxy)benzofuran | HCID 13729408 | — |
反応手順
There was suspended 2.3 g of 2-carbamoyl-7-(2,3-epoxypropoxy)benzofuran obtained in Reference Example 1 in 70 ml of chloroform, and thereto 15 ml of concentrated hydrochloric acid was added. Thereafter, the mixture was vigorously stirred at room temperature for 15 minutes. After the chloroform layer was washed with water and dried with magnesium sulfate, the solvent was distilled away from the reaction mixture under reduced pressure. The resultant residue was purified by silica-gel chromatography (eluent: 2 % ethanol-chloroform) to give the desired compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04652566 |
| 出典データセット | uspto-grants-1987_03 |
| ORD ID | ord-00a4f93f0c5e423b940f80ea6c6f94fd |
| 出典メモ | uspto-grants-1987_03 |