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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741048Generated: October 26, 2026

Hexane → 4-Borono-3-methylbenzoic acid

https://huagongshe.com/reaction/1741048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant4-Bromo-3-methylbenzoic acidHCID 82131—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Borono-3-methylbenzoic acidHCID 2211589273.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A stirred solution of 4-bromo-3-methylbenzoic acid (5.0 g, 0.02 mole) in dry THF (250 ml) at -78° C. under argon was treated with 1.6M n-butyllithium in hexane (36.3 ml, 0.05 mole). The mixture changed from a clear solution to an orange suspension. This was stirred at -78° C. for 0.25 h, then treated with triisopropyl borate (13.4 ml, 0.05 mole) and stirred at -78° C. for a further 1 h. The mixture was allowed to warm to room temp. and stir for 19 h, then treated with water (25 ml) and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 10% methanol/dichloromethane to afford the title compound as a white solid (2.63 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972951
Source datasetuspto-grants-1999_10
ORD IDord-c0a83057945c473bb1fa9471038772e5
Source noteuspto-grants-1999_10