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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720746Generated: October 30, 2026

1-Phenethylamine, (+)- → HCID 60123694, compound

https://huagongshe.com/reaction/720746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenethylamine, (+)-HCID 643189—
Reactant6,7-Dihydro-5H-quinoline-8-oneHCID 11744777—
Catalyst1-Phenethylamine, (+)-HCID 643189—
SolventMethanolHCID 887—
ProductHCID 60123694HCID 60123694104.8%

Reaction Steps

To a stirred solution of 6,7-dihydro-5H-quinolin-8-one (3.02 g, 20.5 mmol) in dry MeOH (100 mL) was added (R)-(+)-α-methylbenzylamine (2.61 mL, 20.5 mmol) via syringe. The resulting mixture was stirred 24 h, at which point additional (R)-(+)-α-methylbenzylamine (0.26 mL, 2.0 mmol) was added and the reaction was stirred for an additional 24 h. The solvent was removed in vacuo and dried for 3 days at room temperature under reduced pressure (0.1 Torr) to afford 5.38 g (95%) of the title compound as a red/brown solid. [α]D=−126.0 (c 1.04, CHCl3); 1H NMR (CDCl3) δ 1.55 (d, 3H, J=6.9 Hz), 2.17–2.29 (m, 2H), 7.35 (t, 2H, J=7.8 Hz), 4.39 (q, 1H, J=6.6 Hz), 4.72 (t, 1H, J=4.7 Hz), 5.50 (br s, 1H), 7.07 (dd, 1H, J=7.5, 5.1 Hz) 7.20–7.47 (m, 6H), 8.37 (d, 1H, J=2.4 Hz); 3C NMR (CDCl3) δ 21.99, 25.68, 28.29, 53.79, 98.12, 122.43, 126.33, 127.03, 128.92, 132.63, 135.09, 139.47, 146.36, 150.48. ES-MS m/z 251 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135570B2
Source datasetuspto-grants-2006_11
ORD IDord-1eb8a8c91abc40e2904e208c19ce73e7
Source noteuspto-grants-2006_11