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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712942Erstellt: 25. Oktober 2026

Benzaldehyde → 2-(Benzylamino)-1-phenylethanol

https://huagongshe.com/reaction/712942

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
PatentnummerUS09181273B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-e6c8f447cb58439da3299bf4e6d75de5
Quellennotizuspto-grants-2015_11