HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522727Generated: October 27, 2026
Hydrochloric Acid → 3-(Trimethylsilyl)phenylboronic acid
https://huagongshe.com/reaction/1522727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Bromo-3-(trimethylsilyl)benzene | HCID 4167050 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(Trimethylsilyl)phenylboronic acid | HCID 4577181 | 86.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09078330B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-c53b3f26ada4492c9f77b34ae4249640 |
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| Source note | uspto-grants-2015_07 |
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