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Hydrochloric Acid → 6,7-Dimethoxy-1-isochromanmethylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2,2-Diethoxyethylamine | HCID 69524 | — |
| 反応物 | 3,4-Dimethoxyphenethyl alcohol | HCID 81911 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 6,7-Dimethoxy-1-isochromanmethylamine | HCID 12225884 | — |
反応手順
A solution of the starting material of formula II, 3,4-dimethoxyphenethyl alcohol (108 g), described by E. Z. Khafagy and J. P. Lambooy, J. Med. Chem., 9, 936 (1966), and the starting material of formula III, aminoacetaldehyde diethyl acetal (78 g), in dry dioxane (250 ml) is stirred and cooled (ice bath) while being saturated with hydrogen chloride over a period of one hour. The mixture is kept at room temperature for two days. The crystalline precipitate is collected, washed with dry dioxane and then ether to yield the hydrochloric acid addition salt (hydrochloride) of the title compound, m.p. 250°-255° C. (dec.), after recrystallization from methanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04036842 |
| 出典データセット | uspto-grants-1977_07 |
| ORD ID | ord-5b92083a5a6c4be885ccd109305c1dc5 |
| 出典メモ | uspto-grants-1977_07 |