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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 735395Erstellt: 26. Oktober 2026

1-Naphthaldehyde → 1-{(S)-[methyl-((S)-1-phenyl-ethyl)-amino]-naphthalen-1-yl-methyl}-naphthalen-2-ol

https://huagongshe.com/reaction/735395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-NaphthaldehydeHCID 6195—
Edukt2-NaphtholHCID 8663—
Edukt(S)-(-)-N,alpha-DimethylbenzylamineHCID 2060073—
LösungsmittelMethanolHCID 887—
Produkt1-{(S)-[methyl-((S)-1-phenyl-ethyl)-amino]-naphthalen-1-yl-methyl}-naphthalen-2-olHCID 1122382351%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

1-Naphthaldehyde (2.7 mL, 20 mmol), (S)-(−)-N,α-dimetylbenzylamine (2.60 g, 19 mmol) and 2-naphthol (2.43 g, 16 mmol) are charged into a 25 mL flask with a magnetic stirring bar. The mixture is heated to 85° C. and stirred for 72 h. After the system is cooled to RT, MeOH (5 mL) is added and the precipitated product is collected by filtration, washed with MeOH (5 mL) and dried to afford 1-{(S)-[methyl-((S)-1-phenyl-ethyl)-amino]-naphthalen-1-yl-methyl}-naphthalen-2-ol as white crystals (about 51% yield): 1H NMR (500 MHz, CDCl3) δ 14.01 (br s, 1H), 7.77-7.02 (m, 18H), 6.45 (s, 1H), 4.40 (br s, 1H), 1.95 (s, 3H), 1.65 (br s, 3H); MS (EI) m/z (rel intensity) 418 (M++1), 283, 141, 136; HRMS (EI) Calcd for C30H28NO (M++1): 418.2171, found 418.2135.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592487B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-2f55e3e8972c41f694b8b10764232ea7
Quellennotizuspto-grants-2009_09