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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753206Generated: November 1, 2026

N-bromobutanimide → 3-Bromo-2-methoxy-5-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1753206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-5-(trifluoromethyl)pyridineHCID 2775312—
SolventAcetonitrileHCID 6342—
Product3-Bromo-2-methoxy-5-(trifluoromethyl)pyridineHCID 1483701834.7%

Reaction Steps

To a stirred solution of 2-methoxy 5-(trifluoromethyl) pyridine (4 g, 22.58 mmol) was dissolved in acetonitrile (50 ml) was added NBS (6 g, 33.87 mmol) portion wise at 0° C. The reaction mixture was stirred for overnight at RT. The solvent was removed under vacuum, quenched with water (100 mL) and extracted with ethyl acetate. The combined organic layer was washed with water, brine, dried over sodium sulfate, and concentrated at reduced pressure to yield 3-bromo-2-methoxy-5-(trifluoromethyl)pyridine (12) as a pale yellow liquid (2 g, 34.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163020B2
Source datasetuspto-grants-2015_10
ORD IDord-f8f8aec63b0142a99d32b4aa9a984ed3
Source noteuspto-grants-2015_10