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HRID 51284Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanone, 1-phenyl-, dihydroxy deriv.HCID 99611—
EduktTert-butyl 4-aminophenethylcarbamateHCID 382207—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
ProduktN-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)anilineHCID 2195986291%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713651B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-58e5785065db4a12bbed314d206e0225
Quellennotizuspto-grants-2004_03