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HRID 275488作成日:2026年10月26日

Aluminium lithium hydride → 3-Cyclopentyloxy-4-methoxyphenethylamine

https://huagongshe.com/reaction/275488

反応式

関与物質

役割名称HCID仕込み量
反応物Aluminium lithium hydrideHCID 21226445—
反応物2-(Cyclopentyloxy)-1-methoxy-4-(2-nitroethenyl)benzeneHCID 54503224—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Cyclopentyloxy-4-methoxyphenethylamineHCID 1127639481%

反応手順

To a suspension of lithium aluminum hydride (10.83 g, 28.5 mmol) in ether (250 mL) at 0° C. under an argon atmosphere was added dropwise a solution of 3-cyclopentyloxy-4-methoxy-β-nitrostyrene (15.00 g, 57.0 mmol) in tetrahydrofuran (85 mL). The resulting mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was cooled to 0° C. and quenched by the successive dropwise addition of water (11 mL), 15% sodium hydroxide (11 mL) and water (33 mL). The mixture was filtered through a pad of Celite™ and the filtrate was washed successively with water, 10% hydrochloric acid and water. The aqueous washes were combined, made basic with saturated aqueous potassium carbonate and extracted three times with ether and twice with methylene chloride. The organic layers were combined and dried (potassium carbonate). Removal of the solvent in vacuo provided the amine (10.80 g, 81%). A portion of the crude amine was purified by flash chromatography, eluting with 1:10:90 water/methanol/chloroform.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393788
出典データセットuspto-grants-1995_02
ORD IDord-940e1276a546428c810a1f12135aa62c
出典メモuspto-grants-1995_02