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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 321895Generated: October 30, 2026

3,4-Difluorobenzeneboronic acid → HCID 131722469, compound

https://huagongshe.com/reaction/321895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Difluorobenzeneboronic acidHCID 2734337—
ReactantHCID 18513409HCID 18513409—
ReactantHCID 22007974HCID 22007974—
ProductHCID 131722469HCID 131722469—

Reaction Steps

The same procedures as in the fourth step were repeated with the exception that 4.3 g (8.9 mmol) of the 4′-(2-(4-propylphenyl)ethyl)-2′,3,5-trifluoro-4-iodobiphenyl obtained in the fifth step was used in place of the 3-fluoro-4-iodo-(2-(4-propylphenyl)ethyl)benzene used in the fourth step, and that 2.1 g (13.3 mmol) of dihydroxy(3,4-difluorophenyl)borane was used in place of dihydroxy(3,5-difluorophenyl)borane, to obtain 3.4 g of a crude 2″,2′,6′,3,4-pentafluoro-4″-(2-(4-propylphenyl)ethyl)terphenyl. This product was recrystallized from mixed solvent of ethanol/ethyl acetate (8/2) to obtain 2.6 g of the subject compound. (Yield: 62.3%) Phase transition temperatures of this product were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06210603B1
Source datasetuspto-grants-2001_04
ORD IDord-b2f12b4f404b49d39a0d9ee149f237b9
Source noteuspto-grants-2001_04