Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68255Erstellt: 23. Oktober 2026

Dichloromethane → 2-(Benzyl(methyl)amino)ethyl acetate

https://huagongshe.com/de/reaction/68255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktAcetic AnhydrideHCID 7918—
EduktTriethylamineHCID 8471—
EduktN-Benzyl-N-methylethanolamineHCID 66876—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt2-(Benzyl(methyl)amino)ethyl acetateHCID 1476145487,5%

Reaktionsschritte

To a 500 mL dry round bottom flask were added 2-(benzyl(methyl)amino)ethanol (46.3 g, 280.2 mmol), triethylamine (150 mL, 1.08 mol), acetic anhydride (31.8 mL, 336.2 mmol), anhydrous CH2Cl2 (100 mL) and a crystal piece of DMAP (4-Dimethylaminopyridine). The mixture was stirred at room temperature for 3 hours. MTBE (700 mL) was added into the reaction mixture, and this mixture was washed, respectively, with cold 2N NaOH (150 mL), water (100 mL), brine (150 mL). The MTBE layer was concentrated, and the residue was poured onto a silica gel pad (200.0 g). The pad was eluted with a co-solvents of ethyl acetate: heptane=3:1 to give 2-(benzyl(methyl)amino)ethyl acetate (50.8 g) as a yellow oil. Yield: 87%. 1H NMR (CDCl3, 300 MHz): δ=7.41-7.25 (m, 5H), 4.29 (t, J=6.3 Hz, 2H), 3.65 (s, 2H), 2.74 (t, J=6.0 Hz, 2H), 2.38 (s, 3H), 2.14 (s, 3H). 13C NMR (CDCl3, 75.5 MHz): δ=170.9, 138.7, 128.9, 128.2, 127.1, 62.5, 62.2, 55.3, 42.6, 21.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822435B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-06eb02ba99414ce280872ed9b8f58245
Quellennotizuspto-grants-2014_09