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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079542Generated: October 31, 2026

Water → 4-(2-Methoxy-ethoxymethoxy)-3-trifluoromethyl-phenyl-boronic acid

https://huagongshe.com/reaction/2079542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriisopropyl borateHCID 21531—
Reactant4-Bromo-1-(2-methoxy-ethoxymethoxy)-2-trifluoromethyl-benzeneHCID 57657555—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methoxy-ethoxymethoxy)-3-trifluoromethyl-phenyl-boronic acidHCID 57657573—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium (2.5M in hexane, 91.2 ml) was added dropwise to a solution of 4-bromo-1-(2-methoxy-ethoxymethoxy)-2-trifluoromethyl-benzene (30 g) in dry THF (335 ml) at −78° C. under nitrogen atmosphere. The mixture was then stirred at −78° C. for another 30 minutes. Triisopropyl borate (101 ml) was then added slowly at −78° C. under nitrogen, the mixture was then allowed to slowly warm up to room temperature and stirred at this temperature overnight. After adding water (300 ml), the mixture was extracted with ethyl acetate (300 ml×3). The combined organic layers were dried over sodium sulphate. After removal of solvent under reduced pressure, the residue was columned on silica gel using DCM-MeOH as eluant to give 4-(2-methoxy-ethoxymethoxy)-3-trifluoromethyl-phenyl-boronic acid (14.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932251B2
Source datasetuspto-grants-2011_04
ORD IDord-b494dd218ca044c2a40836bc4fbfaae9
Source noteuspto-grants-2011_04