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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356090Generated: October 30, 2026

Hydrochloric Acid → 3,5-Dimethylphenylboronic acid

https://huagongshe.com/reaction/356090

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 2M 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 (6 H, s), 7.23 (1 H, s), 7.84 (2 H, s); 13C NMR (CD3OD) 21.36, 133.28, 134.39, 137.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834434
Source datasetuspto-grants-1998_11
ORD IDord-c3df1a0fa4e444c6a7e340f3be7ebe3e
Source noteuspto-grants-1998_11