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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739141Generated: November 2, 2026

Hydrochloric Acid → 3,5-Dimethylphenylboronic acid

https://huagongshe.com/reaction/1739141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantTriisopropyl borateHCID 21531—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
SolventTetrahydrofuranHCID 8028—
Product3,5-Dimethylphenylboronic acidHCID 2734349—

Reaction Steps

Mg turnings (1.44 g, 59.43 mmol) were covered with dry THF (18.8 ml) in a dried, N2 filled flask fitted with an addition funnel and reflux condenser. To this was added 5-bromo-m-xylene (10 g, 54.03 mmol) in THF (15 ml) after initiation of the Grignard reaction. The addition was carried out over several minutes and the reaction mixture was heated at reflux for 1-2 h until most of the Mg had reacted. The reaction mixture was then cooled and transferred to an addition funnel fitted to a N2 filled flask containing triisopropyl borate (24.9 ml) at -70° C. The dropwise addition was carried out over several minutes and the mixture warmed to room temperature and stirred overnight. The grey solution was poured onto 2 M HCl and immediately turned yellow. The solution was extracted into Et2O and the Et2O fractions were combined, dried over MgSO4 and the solvent was removed in vacuo to yield 2.41 g (29.7%). mp 249-251° C.; 1H NMR (CDCl3) 2.44 (6H, s), 7.23 (1H, s), 7.84 (2H, s); 13C NMR (CD3OD) 21.36, 133.28, 134.39, 137.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965539
Source datasetuspto-grants-1999_10
ORD IDord-d496859f02a54a9cb4160aad46c579e9
Source noteuspto-grants-1999_10