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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347869Generated: October 25, 2026

Trimethyl borate → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/reaction/347869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 23080945—

Reaction Conditions

Temperature-10 °C

Reaction Steps

n-Butyllithium (2.64M hexane solution; 182 mL) was added dropwise to a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (121.3 g) in tetrahydrofuran (730 mL) at −78° C., and the mixture was stirred for 20 minutes. A solution of trimethoxyborane (61.7 mL) in tetrahydrofuran (20 mL) was then added to the reaction mixture at −78° C. When internal temperature was raised to −10° C., to the reaction mixture was added saturated aqueous ammonium chloride (730 mL), and stirring was continued for 15 minutes. The obtained reaction mixture was extracted with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (90.4 g) was obtained as a white solid from the n-hexane:ethyl acetate (2:3) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176216B2
Source datasetuspto-grants-2007_02
ORD IDord-98cd5e7682ec4cf5b59bbbfda0652f27
Source noteuspto-grants-2007_02