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1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazine → 1-(2-Bromo-4-methoxyphenyl)piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazine | HCID 23288818 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 生成物 | 1-(2-Bromo-4-methoxyphenyl)piperazine | HCID 23288928 | — |
反応手順
A mixture of 1-formyl-4-(2-bromo-4-methoxyphenyl)piperazine (VII, 3.92 g, 3.1 mmol) and hydrochloric acid (4N, 70 ml) is heated at 100° for 50 min. The mixture is then concentrated under reduced pressure to remove most of the aqueous hydrochloric acid. Saturated sodium bicarbonate is then cautiously added and the aqueous phase is extracted with dichloromethane. The combined organic phase is backwashed with saline, dried over magnesium sulfate, and concentrated to give 1-(2-bromo-4-methoxyphenyl)piperazine (VIII), NMR (CDCl3) 2.55, 2.95, 3.08, 3.77, 6.83, 7.01, 7.14 δ.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05877317 |
| 出典データセット | uspto-grants-1999_03 |
| ORD ID | ord-adba3b0f6a4f4aa382e2cf38ed387201 |
| 出典メモ | uspto-grants-1999_03 |