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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053280Generated: October 25, 2026

3-Fluorophenylboronic acid → (3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic Acid Ethyl Ester

https://huagongshe.com/reaction/2053280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant[3-(5-Bromo-2-fluoro-benzoylamino)-phenoxy]-acetic acid ethyl esterHCID 40356283—
Product(3-[(4,3'-Difluoro-biphenyl-3-carbonyl)-amino]-phenoxy}-acetic Acid Ethyl EsterHCID 59654725—

Reaction Steps

The phenyl bromide (139)(100 mg, 0.25 mmol) was coupled to 3-fluoro-phenylboronic acid (34 mg, 0.24 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. For the ester: LC/MS tr 1.62 min; MS(ES+) m/z 412 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326732B2
Source datasetuspto-grants-2008_02
ORD IDord-76be9de7c11b4505b62e0bfa1cb75589
Source noteuspto-grants-2008_02