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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604603Generated: October 25, 2026

Trimethyl borate → 5-(tert-Butyl)-2-methoxybenzeneboronic acid

https://huagongshe.com/reaction/604603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant4-Tert-butyl-2-iodo-1-methoxybenzeneHCID 14914462—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-(tert-Butyl)-2-methoxybenzeneboronic acidHCID 14740579—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-tert-butyl-2-iodo-1-methoxybenzene (0.164 g, 0.56 mmol) in dry THF (5 mL) at −78° C., n-butyl lithium (0.27 mL, 0.68 mmol, 2.5 M) was added. The solution was stirred at −78° C. for 30 min. Trimethyl borate (0.19 mL, 1.70 mmol) was added. The solution was stirred at −78° C. for 3 h. The reaction was quenched with saturated aqueous NH4Cl. The aqueous layer was extracted with EtOAc (3×15 mL). The combined EtOAc layers were dried over Na2SO4. The residue was used without further purification after evaporation of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-dfe5c271b00d45bc8ac467ae3c6fd1e8
Source noteuspto-grants-2011_03