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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717088Generated: November 3, 2026

3,5-Bis-trifluoromethylphenylboronic acid → 3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phenyl)-acrylic acid ethyl ester

https://huagongshe.com/reaction/1717088

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
Reactant3-{3-[(5-Bromo-furan-2-carbonyl)-amino]-phenyl}-acrylic acid ethyl esterHCID 68494560—
Product3-(3-{[5-(3,5-Bis-trifluoromethyl-phenyl)-furan-2-carbonyl]-amino}phenyl)-acrylic acid ethyl esterHCID 72348811—

Reaction Conditions

Temperature100 °C

Reaction Steps

The furyl bromide (99) (70 mg, 0.19 mmol) was coupled to 3,5-bis-trifluoromethyl-phenylboronic acid (55 mg, 0.21 mmol) acid using Method E, except that the reaction was heated at 100° C. The crude product was purified by column chromatography eluting with a stepped gradient of 0-10% EtOAc in heptane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803841B2
Source datasetuspto-grants-2010_09
ORD IDord-c7c2360b81fc444c895edba4d0ff4bfe
Source noteuspto-grants-2010_09