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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275488생성일: 2026년 10월 24일

Aluminium lithium hydride → 3-Cyclopentyloxy-4-methoxyphenethylamine

https://huagongshe.com/ko/reaction/275488

반응식

참여 물질

역할이름HCID투입량
반응물Aluminium lithium hydrideHCID 21226445—
반응물2-(Cyclopentyloxy)-1-methoxy-4-(2-nitroethenyl)benzeneHCID 54503224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Cyclopentyloxy-4-methoxyphenethylamineHCID 1127639481%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393788
출처 데이터셋uspto-grants-1995_02
ORD IDord-940e1276a546428c810a1f12135aa62c
출처 메모uspto-grants-1995_02