Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422364Generated: October 31, 2026

Tributyl borate → (2-ethyl-4-methoxyphenyl)boronic acid

https://huagongshe.com/reaction/2422364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyl borateHCID 12712—
Reactant1-BROMO-2-ETHYL-4-METHOXY-BENZENEHCID 12386619—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2-ethyl-4-methoxyphenyl)boronic acidHCID 11506554—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-bromo-3-ethyl anisole (94 g, 0.437 mol) in THF (900 ml) was cooled to −78° C. n-Butyl lithium (249 ml, 0.55 mol) was added dropwise at the same temperature. Stirring was continued for 1 hr at −78° C. Tri-n-butyl borate (177 ml, 0.655 mol) was added slowly at −78° C. The cooling bath was removed, the reaction mixture was allowed to warm to 0° C. and was quenched with 1.5 N hydrochloric acid at 0° C. The organic layer was separated. The aqueous layer was extracted with ethylacetate and the combined organic layers were washed with brine and concentrated. The residue obtained was stirred in petroleum ether for 30 min. The solid obtained was filtered and dried under vacuum. Yield: 65 g, 82%, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960349B2
Source datasetuspto-grants-2011_06
ORD IDord-79297b6526e8447bbf326fd1a6530edc
Source noteuspto-grants-2011_06