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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896054Generated: November 4, 2026

N,N-Dimethylaniline → 2-bromo-N-[2,4-bis(2,2,2-trifluoroethoxy)-6-methylpyridin-3-yl]acetamide

https://huagongshe.com/reaction/1896054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantBromoacetyl bromideHCID 61147—
Reactant3-Amino-2,4-bis(2,2,2-trifluoroethoxy)-6-methyl-3-nitropyridineHCID 23092432—
SolventDichloromethaneHCID 6344—
Product2-bromo-N-[2,4-bis(2,2,2-trifluoroethoxy)-6-methylpyridin-3-yl]acetamideHCID 1158993085%

Reaction Steps

3-Amino-2,4-bis(2,2,2-trifluoroethoxy)-6-methyl-3-nitropyridine (42.29 g, 139.0 mmol) was dissolved in dichloromethane (600 mL), followed by the addition of N,N-dimethylaniline (20.46 g, 16.8 mmol). While stirring the mixture in an ice bath, a solution of bromoacetyl bromide (28.73 g, 142.3 mmol) in dichloromethane (100 mL) was added dropwise, and the reaction mixture was stirred at room temperature for 10 minutes. The reaction mixture was extracted with chloroform-water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was recrystallized from chloroform-hexane to obtain the title compound (50.25 g, 85%) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518936B2
Source datasetuspto-grants-2013_08
ORD IDord-0ccebef96cd3486f837a1f6bcd1197d2
Source noteuspto-grants-2013_08