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HRID 63075作成日:2026年10月27日

6-Methoxy-alpha-tetralone → 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/63075

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methoxy-alpha-tetraloneHCID 14112—
反応物Sodium HydroxideHCID 14798—
反応物Trimethylsilyl cyanideHCID 82115—
反応物Aluminium lithium hydrideHCID 21226445—
触媒zinc(II)iodideHCID 9883512—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 1319758968.4%

反応条件

温度60 °C

反応手順

TMS-cyanide (8.52 mL, 68.1 mmol) was added to a solution of 6-methoxy-1-tetralone (6.0 g, 34 mmol) in toluene (50 mL). A trace amount (˜20 mg) of zinc iodide was added, and the reaction was stirred at 60° C. for 16 hours. The solution was cooled to rt and diluted with THF (30 mL). This was added to a mixture of lithium aluminum hydride (2.58 g) in THF (50 mL), and the reaction mixture was heated at 42° C. for 2 h. The reaction was cooled to rt. EtOAc (10 mL) was slowly added, and the reaction stirred 30 min. Water (2 mL) and then 5N NaOH (1 mL) were slowly added, and the reaction stirred 1 h. The reaction mixture was diluted with EtOAc (100 mL), dried (MgSO4), and filtered through Celite. Purification by silica gel chromatography (10-20% MeOH/DCM) gave 4.82 g of 1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447045B2
出典データセットuspto-grants-2016_09
ORD IDord-060b901605a7488ead9bd01c7620fa71
出典メモuspto-grants-2016_09