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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75147생성일: 2026년 10월 23일

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol

https://huagongshe.com/ko/reaction/75147

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
반응물2-[4-(Benzyloxy)phenyl]oxiraneHCID 13248717—
용매IsopropanolHCID 3776—
생성물1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanolHCID 5943717623.2%

반응 단계

2-(4-(benzyloxy)phenyl)oxirane (2 g, 8.8 mmol) and (1-adamantylmethyl)amine (1.46 g, 8.8 mol) were dissolved in isopropyl alcohol (30 mL) and heated under reflux overnight. The mixture was concentrated to give the crude product, which was purified by column chromatography to afford 1-(4-(benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol (0.8 g, 23%). 1H NMR: (CDCl3, 400 MHz) δ=1.51 (m, 6H), 1.60-1.72 (m, 6H), 1.97 (m, 3H), 2.32&2.45 (dd, 2H), 2.64 (m, 1H), 2.73 (m, 1H), 2.94 (m, 1H), 3.40 (brs, 3H), 4.79 (m, 1H), 6.93 (m, 2H), 7.26-7.43 (m, 7H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835426B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-88047b6c7522438b9fa11d82686d0f95
출처 메모uspto-grants-2014_09