化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1194349作成日:2026年10月25日
Formaldehyde → 3-(Dimethylamino)-1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-propanone hydrochloride hemihydrate
https://huagongshe.com/reaction/1194349
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Dimethylamine, hydrochloride | HCID 10473 | — |
| 反応物 | 1-(5-Methoxy-1-methyl-1H-indol-3-yl)ethan-1-one | HCID 21270028 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-(Dimethylamino)-1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-propanone hydrochloride hemihydrate | HCID 70045959 | — |
反応手順
A mixture of 1-(5-methoxy-1-methyl-1H-indol-3-yl)-1-ethanone (0.23 g), paraformaldehyde (0.07 g) and dimethylamine hydrochloride (0.2 g) in ethanol (20 ml) was heated at reflux for 24 h, cooled, and the solvent was evaporated in vacuo. The residue was partitioned between sodium carbonate (2N; 50 ml) and ethyl acetate (2×50 ml). The combined organic extracts were dried and evaporated in vacuo to give an oil, which was purified by FCC eluting with System A to give the free base of the title compound as an oil. This was dissolved in absolute ethanol (5 ml) acidified with ethanolic hydrogen chloride, and the salt was precipitated by the addition of excess dry ether (100 ml). The salt was filtered off and dried in vacuo to give the title compound (0.1 g), m.p. 210°-211°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04814344 |
|---|
| 出典データセット | uspto-grants-1989_03 |
|---|
| ORD ID | ord-9b9d20f39774446f835bc8e0b6fc8660 |
|---|
| 出典メモ | uspto-grants-1989_03 |
|---|