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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480606Generated: October 26, 2026

Hexane → (5-(Tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acid

https://huagongshe.com/reaction/1480606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTrimethyl borateHCID 8470—
Reactant2-Bromo-4-(tert-butyl)-1-((2-methoxyethoxy)methoxy)benzeneHCID 86718561—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(5-(Tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acidHCID 8671856298%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium in hexane (2.5 M, 4.2 mL, 10.5 mmol) was added dropwise to a solution of give 2-bromo-4-(tert-butyl)-1-((2-methoxyethoxy)methoxy)benzene (3.0 g, 9.46 mmol) and trimethyl borate (1.2 mL, 10.76 mmol) in anhydrous tetrahydrofuran (20 mL) at −78° C. under nitrogen. The reaction mixture was stirred at −78° C. for 20 minutes then at 0° C. for an additional 20 minutes. The reaction was then quenched by the addition of water (20 mL) and the mixture extracted with ether (100 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated under reduced pressure to give (5-(tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acid (2.61 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409893B2
Source datasetuspto-grants-2016_08
ORD IDord-9c91b4d9823442dd9003c41390c58839
Source noteuspto-grants-2016_08