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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392828Generated: October 25, 2026

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

https://huagongshe.com/reaction/392828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantN-BenzylphenethylamineHCID 65055—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-N-(2-phenylethyl)acetamideHCID 8032171102.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803378B2
Source datasetuspto-grants-2004_10
ORD IDord-7edcf815d4114aaa94c7bd9a5fb72a12
Source noteuspto-grants-2004_10