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Potassium Carbonate → Benzaldehyde, 2-(3-(4-phenyl-1-piperazinyl)propoxy)-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-(3-Chloropropyl)-4-phenylpiperazine dihydrochloride | HCID 12399682 | — |
| 反応物 | Sodium 2-formylbenzenolate | HCID 86741752 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Benzaldehyde, 2-(3-(4-phenyl-1-piperazinyl)propoxy)- | HCID 55232 | 74.4% |
反応手順
A mixture of 3.88 g of 2-hydroxybenzaldehyde sodium salt, 7.00 g of 1-(3-chloropropyl)-4-phenylpiperazine dihydrochloride, 6.80 g of potassium carbonate and 50 ml of dimethylformamide is stirred at 60° to 70° C. for 15 hours under nitrogen atmosphere, and is concentrated under reduced pressure to remove solvent. Water is added to the residue, and the aqueous mixture is extracted with ether. The extract is washed with water, dried and concentrated under reduced pressure to remove solvent. The residue is purified by silica gel chromatography (solvent, chloroform:methanol=99:1). 5.42 g of 2-[3-(4-phenylpiperazin-1-yl)propyloxy]benzaldehyde are obtained as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04689327 |
| 出典データセット | uspto-grants-1987_08 |
| ORD ID | ord-84c56ccc3d8f4af7b42a8396c4f681d0 |
| 出典メモ | uspto-grants-1987_08 |