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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51284생성일: 2026년 10월 24일

Ethanone, 1-phenyl-, dihydroxy deriv. → N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)aniline

https://huagongshe.com/ko/reaction/51284

반응식

참여 물질

역할이름HCID투입량
반응물Ethanone, 1-phenyl-, dihydroxy deriv.HCID 99611—
반응물Tert-butyl 4-aminophenethylcarbamateHCID 382207—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)anilineHCID 2195986291%

반응 단계

4-(N-Boc-2-aminoethyl)aniline 28 (1.25 g, 5.29 mmole) was dissolved in methanol (30 mL), followed by addition of phenyl glyoxal 24 (0.708 g, 5.28 mmole). The reaction mixture was stirred for 1 h at rt, prior to addition of NaCNBH3 (0.665 g, 10.6 mmole). The final mixture was stirred for 12 h at rt, concentrated, and purified by flash silica column chromatography (2 to 5% MeOH/CH2Cl2) to give N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)-aniline as a pale yellow oil (1.71 g, 91%): Rf=0.18 in 5% MeOH/CH2Cl2. 1H-NMR (CD3OD, 299.96 MHz): δ (ppm) 7.4-7.25 (m, 5H), 7.0-6.95 (d, 2H), 6.63-6.60 (d, 2H), 4.85-4.79 (dd, 1H), 3.3-3.21 (t, 2H), 3.2-3.15 (m, 2H), 2.64-2.5 (t, 2H), 1.42 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713651B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-58e5785065db4a12bbed314d206e0225
출처 메모uspto-grants-2004_03