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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72862Erstellt: 24. Oktober 2026

Benzaldehyde → 2-(Benzylamino)-1-phenylethanol

https://huagongshe.com/de/reaction/72862

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPhenylethanolamineHCID 1000—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
Produkt2-(Benzylamino)-1-phenylethanolHCID 22974670,4%

Reaktionsschritte

To a solution of 2-amino-1-phenyl-ethanol (12.0 g, 87.48 mmol) in methanol (60 mL) was added benzaldehyde (9.3 g, 8.9 mL, 87.48 mmol) and the reaction mixture was stirred for 1 hour at room temperature. The reaction mixture was then cooled to 0° C. and sodium borohydride (3.3 g, 87.48 mmol) was added. The reaction mixture was gradually allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated in vacuo, diluted with water, and filtered. The residue was rinsed with cold isopropanol (3×), then dried in vacuo to give 2-(benzylamino)-1-phenylethanol as white crystals (14.0 g, 70%). ESI-MS m/z calc. 227.1. Found 228.2 (M+1)+; Retention time:0.8 minutes (3 min run). 1H NMR (400 MHz, MeOD) δ 7.37-7.27 (m, 8H), 7.27-7.19 (m, 2H), 4.78 (dd, J=8.5, 4.5 Hz, 1H), 3.77 (q, J=13.0 Hz, 2H), 2.82-2.68 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828996B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-aed35b26e3794dc99f4e65ea0289b1f7
Quellennotizuspto-grants-2014_09