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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028637Generated: October 31, 2026

Triisopropyl borate → 2-Methoxy-5-(trifluoromethyl)phenylboronic acid

https://huagongshe.com/reaction/1028637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant2-iodine-4 -(trifluoromethyl) anisoleHCID 18706296—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-5-(trifluoromethyl)phenylboronic acidHCID 2782676—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium (1.6M in hexanes, 456 μL, 0.729 mmol) was added dropwise to a stirred solution of 2-iodo-1-methoxy-4-(trifluoromethyl)benzene (Step A, 200 mg, 0.662 mmol) in THF (1.5 mL) at −78° C. under an atmosphere of nitrogen. The reaction stirred at −78° C. for 30 min prior to the addition of triisopropyl borate (458 μL, 1.986 mmol). The reaction stirred an additional 2 h at −78° C. and was quenched with sat. NH4Cl. The mixture was extracted with CH2Cl2 and the organic phase was washed with NaHCO3 (15 mL) and brine (15 mL), dried (Na2SO4), filtered, conc. in vacuo to afford [2-methoxy-5-(trifluoromethyl)phenyl]boronic acid which was carried on without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-3cd4d6b95d6541fdb506a31e7bbe2ed8
Source noteuspto-grants-2014_05