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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096913Generated: October 29, 2026

Acetaldehyde → 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide

https://huagongshe.com/reaction/2096913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantTriethylamineHCID 8471—
ReactantHCID 23649017HCID 23649017—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-acetylamino-N-benzyl-3-difluoromethoxy-propionamideHCID 2364901659.1%

Reaction Steps

To a solution of 2-amino-N-benzyl-3-(difluoromethoxy)propanamide (195 mg, 0.798 mmol) and triethylamine (322 mg, 3.19 mmol) in THF (5 mL), acetic hydride (98.5 mg, 0.958 mmol) was added. The reaction mixture was stirred at room temperature for an hour, diluted with ethyl acetate and washed with water. The organic layer was concentrated with silica gel and purified by column chromatography, eluting with 50-100% ethyl acetate in hexanes. The product was triturated with diethyl ether to give 2-(acetylamino)-N-benzyl-3-(difluoromethoxy)propanamide (135 mg, 59%) as a white solid, MP: 173.3° C. 1H NMR (300 MHz, CDCl3): (ppm) 7.25-7.39 (m, 5H), 6.68 (w, 1H), 6.42 (d, 1H), 6.24 (wt, 1H), 4.73 (m, 1H), 4.48 (d, 2H), 4.24 (dd, 1H), 4.01 (dd, 1H) and 2.05 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450336B2
Source datasetuspto-grants-2013_05
ORD IDord-2a4a3d689832441a826da6f16c0731de
Source noteuspto-grants-2013_05