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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392828Erstellt: 23. Oktober 2026

Acetyl chloride → N-benzyl-N-(2-phenylethyl)acetamide

https://huagongshe.com/de/reaction/392828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktN-BenzylphenethylamineHCID 65055—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-benzyl-N-(2-phenylethyl)acetamideHCID 8032171102,6%

Reaktionsschritte

N-benzyl-2-phenethylamine (2.2 g, 10 mmol) was dissolved in 7 mL of CH2Cl2. To this was added 7 mL of satd (aq.) NaHCO3 followed by acetyl chloride (0.88 g, 11 mmol) and the resulting mixture stirred for 40 min. The organic layer was separated, dried over Na2SO4 filtered and the solvent removed to yield 2.60 g (100%) oil. LC/MS (M+H) calcd for C17H20NO: 254.15; found: 254.07. 1H NMR and 13C NMR show a mixture of rotamers at room temperature. 1H NMR (500 MHz, CDCl3), δ: 2.04 (br s), 2.14 (br s), 2.81 (br m), 2.87 (br m), 3.44 (br m), 3.58 (br m), 4.36 (s), 4.62 (s), 7.11-7.36 (overlapping m, 10). 13C NMR (125 MHz, CDCl3) δ: 21.19, 21.80, 33.99, 34.87, 48.18, 48.28, 49.49, 52.75, 126.34, 126.81, 127.44, 127.65, 128.18, 128.52, 128.64, 128.73, 128.80, 128.85, 128.94, 136.74, 137.56, 138.17, 139.24, 170.81, 171.07.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06803378B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-7edcf815d4114aaa94c7bd9a5fb72a12
Quellennotizuspto-grants-2004_10