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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351469Generated: October 25, 2026

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

https://huagongshe.com/reaction/1351469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylglyoxalHCID 14090—
ReactantTert-butyl 4-aminophenethylcarbamateHCID 382207—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductN-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)anilineHCID 2195986291%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217738B2
Source datasetuspto-grants-2007_05
ORD IDord-18fc287f6ae74f5d9a25db91e4a9e298
Source noteuspto-grants-2007_05