돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1351469생성일: 2026년 10월 27일

Phenylglyoxal → N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)aniline

https://huagongshe.com/reaction/1351469

반응식

참여 물질

역할이름HCID투입량
반응물PhenylglyoxalHCID 14090—
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 번호US07217738B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-18fc287f6ae74f5d9a25db91e4a9e298
출처 메모uspto-grants-2007_05