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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027174Generated: October 26, 2026

Trimethyl borate → (4-(1H-imidazol-1-yl)-2-methoxyphenyl)boronic acid

https://huagongshe.com/reaction/1027174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant1-(4-bromo-3-methoxyphenyl)-1H-imidazoleHCID 84707792—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-(1H-imidazol-1-yl)-2-methoxyphenyl)boronic acidHCID 86710567—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 1-(4-bromo-3-methoxyphenyl)-1H-imidazole in THF (5 mL) was added 2.5 M n-butyl lithium in hexanes (0.348 ml, 0.869 mmol) dropwise at −78° C. over 15 min. After addition was complete, the reaction solution was stirred at −78° C. for 15 min, and trimethyl borate (0.353 mL, 3.16 mmol) was added. The reaction was allowed to warm to RT, and continued to stir overnight. The reaction was quenched with 1 M HCl aqueous solution to pH 2, diluted with water and extracted with DCM (3×). The product remained in the aqueous solution which was concentrated in vacuo to give crude (4-(1H-imidazol-1-yl)-2-methoxyphenyl)boronic acid (120 mg, MS: 219.2 [M+H+]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-72ddd791864547208faa52aa37c0a43f
Source noteuspto-grants-2014_05