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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354021Generated: November 1, 2026

Ammonia → 2-bromo-N-(2,6-dimethyl-4-trifluoromethyl-3-pyridyl)acetamide

https://huagongshe.com/reaction/2354021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN,N-DimethylanilineHCID 949—
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 23092424HCID 23092424—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-bromo-N-(2,6-dimethyl-4-trifluoromethyl-3-pyridyl)acetamideHCID 2309243796%

Reaction Steps

3-Amino-2,6-dimethyl-4-trifluoromethylpyridine dihydrochloride (15.60 g, 59.30 mmol) was dissolved in methanol (100 mL). In an ice bath, an ammonia-saturated methanol solution (300 mL) was added, and the mixture was rendered uniform. The reaction mixture was extracted from chloroform-water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was dissolved in dichloromethane (200 mL), and subsequent to the addition of N,N-dimethylaniline (10.80 g, 89.12 mmol), a solution of bromoacetyl bromide (15.52 g, 76.90 mmol) in dichloromethane (40 mL) was added dropwise while stirring the mixture in an ice bath. The mixture was stirred at room temperature for two hours, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (silica gel: 400 g; developer: hexane:acetone=10:1→4:1→3:1). Recrystallization from ethyl acetate and hexane afforded the title compound (17.68 g, 96%) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750150B2
Source datasetuspto-grants-2010_07
ORD IDord-4465750ce7154a5488da3054808329e8
Source noteuspto-grants-2010_07