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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096926Generated: October 31, 2026

Acetic Anhydride → 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide

https://huagongshe.com/reaction/2096926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 23649017HCID 23649017—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-acetylamino-N-benzyl-3-difluoromethoxy-propionamideHCID 2364901659.1%

Reaction Steps

2-Amino-N-benzyl-3-difluoromethoxy-propionamide (195 mg, 0.80) was mixed with triethylamine (322 mg, 3.19 mmol) in THF (5 mL). Acetic anhydride (98.5 mg, 0.96 mmol) was then added and the reaction mixture was stirred for 1 hour. The mixture was then diluted with ethyl acetate and washed with water. The organic layer was dried and concentrated. The residue was purified by column chromatography using hexanes:ethyl acetate (50:50 to 0:100). The isolated product was triturated with diethyl ether to give 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide (135 mg, 59%) as a white solid. 1H NMR (300 MHz, CDCl3): δ (ppm) 7.33 (m, 5H), 6.68 (br, 1H), 6.37 (br, 1H), 6.24 (t, 1H), 4.72 (q, 1H), 4.87 (d, 2H), 4.23 (dd, 1H), 4.01 (dd, 1H), 2.05 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450336B2
Source datasetuspto-grants-2013_05
ORD IDord-1307a85cfc8c4372bcb2a3a41416066c
Source noteuspto-grants-2013_05