戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 228874作成日:2026年10月26日

Aminoacetaldehyde dimethyl acetal → 6-Methoxy-7-methylisoquinoline

https://huagongshe.com/reaction/228874

反応式

関与物質

役割名称HCID仕込み量
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物3-Methyl-4-anisaldehydeHCID 122936—
溶媒BenzeneHCID 241—
生成物6-Methoxy-7-methylisoquinolineHCID 2307843822.1%

反応条件

温度-10 °C

反応手順

4-Methoxy-3-methylbenzaldehyde (3.00 g) was dissolved in benzene (30 ml) to prepare a solution. 2,2-Dimethoxy-ethylamine (2.10 g) was added to the solution, and the mixture was heated under reflux overnight. The solvent was removed by distillation under the reduced pressure, the residue was then dissolved in tetrahydrofuran (30 ml), and the mixture was cooled to −10° C. Ethyl chloroformate (2.17 g) and trimethyl phosphite (2.97 g) were added thereto, and mixture was stirred at room temperature overnight. The solvent was removed by distillation under the reduced pressure, the residue was then dissolved in dichloromethane (30 ml), titanium tetrachloride (22.7 g) was added to the solution, and the mixture was heated under reflux for 36 hr. The reaction solution was cooled to room temperature, was then neutralized with a 1 N aqueous sodium hydroxide solution, and was extracted with 3 N hydrochloric acid. The aqueous layer was made basic by the addition of a 3 N aqueous sodium hydroxide solution and was then extracted with dichloromethane. The solvent was removed by distillation under the reduced pressure to give 6-methoxy-7-methylisoquinoline (764 mg, yield 22%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560558B2
出典データセットuspto-grants-2009_07
ORD IDord-8f1ea0b70d5d4e14ae7d2430c5424f85
出典メモuspto-grants-2009_07