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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942670Generated: November 3, 2026

Triisopropyl borate → {2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acid

https://huagongshe.com/reaction/1942670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzeneHCID 58494123—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product{2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acidHCID 58494144—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene (D100) (930 mg, 3.83 mmol) in Tetrahydrofuran (THF) (10 mL) was added BuLi (1.989 mL, 4.97 mmol) dropwise at −78° C. under nitrogen. The reaction mixture was stirred at −78° C. for 2 hours. Tris(1-methylethyl) borate (1.319 mL, 5.74 mmol) was added to the reaction mixture by syringe at −78° C. Then the reaction was stirred at −78° C. for 30 min, and then warmed to room temperature slowly. Then the reaction was quenched with water. The mixture was extracted with EA (15 mL×3). The combined organic layers was dried over anhydrous sodium sulphate. After filtration and concentration, the crude {2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acid (D101) (741 mg) was used directly in the next step. MS (ES): C10H13BO4 requires 208.1. found 209.0 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-7c6bb231cefb4316a39223c4fab26790
Source noteuspto-grants-2013_03