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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502018Generated: October 29, 2026

N-bromobutanimide → 3-Bromo-6-fluoro-2-methoxybenzonitrile

https://huagongshe.com/reaction/1502018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-6-methoxybenzonitrileHCID 523101—
SolventTrifluoromethanesulfonic acidHCID 62406—
Product3-Bromo-6-fluoro-2-methoxybenzonitrileHCID 71270710—

Reaction Steps

2-Fluoro-6-methoxybenzonitrile (8.30 g, 54.9 mmol) was dissolved in Triflic acid (75 mL) at 0° C. then NBS (10.3 g, 57.7 mmol) was added. The reaction mixture was stirred at RT for 1 h. LC-MS showed no starting material peak. The reaction mixture was poured into ice and extracted twice with DCM. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified by chromatography through a 330 g Redi-Sep column and eluted with 10% to 50% EtOAc/hexane solvent system to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-48780755fb014aa7ab36b02c03620474
Source noteuspto-grants-2015_12