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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471459Generated: October 31, 2026

Toluene → (2-Fluoro-4-methylphenyl)boronic acid

https://huagongshe.com/reaction/1471459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTetrahydrofuranHCID 8028—
ReactantTriisopropyl borateHCID 21531—
Reactant4-Bromo-3-fluorotolueneHCID 573280—
SolventHexaneHCID 8058—
Product(2-Fluoro-4-methylphenyl)boronic acidHCID 2783132—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a mixture of toluene (160 ml) and THF (40 ml) are added triisopropyl borate (13.56 ml, 58.42 mmole) and 3-fluoro-4-bromotoluene (10.0 g, 48.69 mmole). The mixture is cooled down to −40° C. and n-Butylithium (2.5M in hexane) (23.4 ml, 58.42 mmole) is added slowly over 1 h and the mixture is stirred for an additional hour while the temperature is held at −40° C. The acetone/dry ice bath is removed and the reaction mixture is allowed to warm to −20° C. before a 2.5M HCl solution (20 ml) is added. When the mixture reached rt, the aqueous layer is extracted with EtOAc(3×50 ml), organic extracts are combined, dried over MgSO4 (anhydrous) and evaporated under reduced pressure to give a yellow solid, which is recrystallised from acetonitrile, affording the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012451B2
Source datasetuspto-grants-2015_04
ORD IDord-06126d1c85eb4c39a4b179b0664c844b
Source noteuspto-grants-2015_04