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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257429Generated: October 27, 2026

Acetyl chloride → 2-Acetamido-5-nitropyridine

https://huagongshe.com/reaction/257429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-5-nitropyridineHCID 77888—
SolventDichloromethaneHCID 6344—
Product2-Acetamido-5-nitropyridineHCID 34512549%

Reaction Steps

To a solution of 2-amino-5-nitropyridine (4.0 g, 28.8 mmol) in dichloromethane (15 ml) were added 176 mg (31.6 mmol) of 4-N,N'-dimethylaminopyridine (DMAP), 4.41 ml of triethylamine (31.6 mmol) and 2.16 ml (31.6 mmol) of acetyl chloride in turn, and the mixture was stirred at room temperature for 1 hour. A 1 M aqueous solution of potassium carbonate was added to the mixed suspension to neutralize it. Extraction with chloroform was repeated three times, and the extract was dried over magnesium sulfate. The solvent was removed, and the residue was subjected to silica gel column chromatography (eluent: chloroform). Recrystallization from chloroform-hexane gave 2.14 g of the intended product as a flesh-colored powder (yield: 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262415
Source datasetuspto-grants-1993_11
ORD IDord-73c9e560c9684380bd116308f47e6239
Source noteuspto-grants-1993_11