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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578760Generated: October 31, 2026

2-Fluorophenylboronic acid → HCID 71259057, compound

https://huagongshe.com/reaction/578760

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorophenylboronic acidHCID 2734354—
ReactantHCID 19828469HCID 19828469—
ProductHCID 71259057HCID 71259057—

Reaction Steps

Subsequently, Suzuki-Miyaura conditions were applied as in FIG. 8 using 2-bromo-5,6,7,8-tetrahydroquinoline and 2-fluorophenylboronic acid to obtain the 2-(2-fluorophenyl)-5,6,7,8-tetrahydroquinoline precursor as depicted in FIG. 10. After isolation and purification by flash chromatography, this viscous yellow-orange liquid solidifies at room temperature. In general, 2-(2-fluorophenyl)-pyridine derivatives wore prepared in high yields (over 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040704B2
Source datasetuspto-grants-2015_05
ORD IDord-6a1677c9eb3a4fa7a26e5118624e0007
Source noteuspto-grants-2015_05