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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522727Generated: October 27, 2026

Hydrochloric Acid → 3-(Trimethylsilyl)phenylboronic acid

https://huagongshe.com/reaction/1522727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-3-(trimethylsilyl)benzeneHCID 4167050—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-(Trimethylsilyl)phenylboronic acidHCID 457718186.4%

Reaction Steps

t-Butyllithium (28 cm3, 1.7 M in pentane) was added to a solution of (21) (9.65 g, 42 mmol) in ether (200 cm3) cooled in a dry ice/acetone bath, and the reaction was stirred for 30 minutes. Trimethyl borate (20 cm3, 170 mmol) was added, and the reaction was stirred for 16 hours, gradually warming to room temperature. Aqueous hydrochloric acid (3 M, 20 cm3) was added, and the reaction was stirred for a further 2 hours. Water (200 cm3) was added, and the layers were separated. The aqueous layer was extracted with ether (3×30 cm3). The combined organic extracts were washed with brine (300 cm3) and dried over magnesium sulfate, and the solvent was removed to leave a white solid. The crude product was passed through a plug of silica using light petroleum then ether as the eluent. The ether band was collected, and the solvent was removed to leave (22) as a brown solid (7.04 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09078330B2
Source datasetuspto-grants-2015_07
ORD IDord-c53b3f26ada4492c9f77b34ae4249640
Source noteuspto-grants-2015_07