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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604224Generated: November 2, 2026

Trimethyl borate → 5-Sec-butyl-1-methoxy-benzene boronic acid

https://huagongshe.com/reaction/604224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-1-methoxy-4-(1-methylpropyl)benzeneHCID 66602978—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Sec-butyl-1-methoxy-benzene boronic acidHCID 86626524—

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Bromo-4-sec-butyl-1-methoxy-benzene (1.15 g) is dissolved in tetrahydrofuran (17 ml) and the mixture is cooled to −78° C., and thereto is added dropwise 1.6M n-butyllithium in hexanes, and the mixture is stirred at −78° C. for 15 minutes. To the reaction solution is added trimethyl borate (1.47 g), and the reaction mixture is stirred at −78° C. for 30 minutes, and thereto are added a saturated aqueous ammonium chloride solution and ethyl acetate. The mixture is separated, and the organic layer is washed with a saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give crude 5-sec-butyl-1-methoxy-benzene boronic acid (950 mg). NMR (CDCl3): 0.81 (3H, t), 1.22 (3H, d), 1.58 (2H, m), 2.58 (1H, m), 3.90 (3H, s), 6.25 (2H, s), 6.85 (2H, d), 7.25 (1H, d), 7.65 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906517B2
Source datasetuspto-grants-2011_03
ORD IDord-41d7710d29104a60b03e11c7c459f28a
Source noteuspto-grants-2011_03