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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444378Generated: October 26, 2026

4-Fluorophenylboronic acid → {3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid ethyl ester

https://huagongshe.com/reaction/1444378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant[3-(5-Bromo-2-fluoro-benzoylamino)-phenoxy]-acetic acid ethyl esterHCID 40356283—
Product{3-[(4,4'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic acid ethyl esterHCID 59654610—

Reaction Steps

The phenyl bromide (139) (100 mg, 0.25 mmol) was coupled to 4-fluoro-phenylboronic acid (33 mg, 0.23 mmol) using Method E. During this reaction, partial hydrolysis occurred. The residue was extracted using Work-up E1 to give a mixture of acid and ester, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662839B2
Source datasetuspto-grants-2010_02
ORD IDord-ddf79c39b9fd41d0bc1b03ded651fa52
Source noteuspto-grants-2010_02