Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17524Generated: October 28, 2026

N-bromobutanimide → 5-Amino-2-bromo-6-fluoro-4-methoxybiphenyl-3-carbonitrile

https://huagongshe.com/reaction/17524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Amino-6-fluoro-4-methoxybiphenyl-3-carbonitrileHCID 86097506—
SolventAcetic AcidHCID 176—
Product5-Amino-2-bromo-6-fluoro-4-methoxybiphenyl-3-carbonitrileHCID 8609750889.5%

Reaction Steps

5-Amino-6-fluoro-4-methoxybiphenyl-3-carbonitrile (I-234) (500 mg, 2.06 mmol) was dissolved in acetic acid (9.5 ml), and at room temperature, N-bromosuccinimide (441 mg, 2.48 mmol) was gradually added. After stirring under nitrogen atmosphere at room temperature for 1 hour, the solvent was evaporated away under reduced pressure. The residue was fractionated with ethyl acetate and aqueous 1M sodium hydroxide solution. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, hexane:ethyl acetate=3:1) to obtain the entitled compound (592 mg, 89%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-618182d5fd9d4d75b4fee67d0e8f90e2
Source noteuspto-grants-2010_06