関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 1-Hydrazinyl-3,4-dihydroisoquinoline | HCID 12349041 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1-(2-Ethylidenehydrazino)-3,4-dihydroisoquinoline | HCID 57269150 | — |
反応手順
A mixture of 1-ethoxy-3,4-dihydroisoquinoline (1.0 g.), hydrazine monohydrochloride (0.4 g.) and absolute ethanol (15 ml.) was heated under reflux (for 40 min.). The solution was cooled, filtered and concentrated and the residue was recrystallized from ethanol-ether, affording 1-hydrazino-3,4-dihydroisoquinoline hydrochloride (0.9 g., m.p. 205°-207° C.). C. A mixture of 1-hydrazino-3,4-dihydroisoquinoline (8.0 g.), acetaldehyde (20 ml.) and ethanol (20 ml.) was allowed to stand at room temperature (for 45 min). Ethanolic sulfuric acid was added until the solution was distinctly acidic. Ether was added. The resulting oil crystallized and the crystals were recrystallized from ethanol-ether, affording 1-(2-ethylidenehydrazino)-3,4-dihydroisoquinoline (I: X=CH3, X'=Y=Y'=Z=Z'=H) sulfate in two crops (8.3 g., m.p. 152°-154° C.; 0.5 g., m.p. 152°-155° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04009170 |
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| 出典データセット | uspto-grants-1977_02 |
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| ORD ID | ord-094a02f11dc94b20987158205f53cf8c |
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| 出典メモ | uspto-grants-1977_02 |
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