HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018809Generated: October 30, 2026
Hydrochloric Acid → (3,5-Difluorophenyl)boronic acid
https://huagongshe.com/reaction/1018809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Bromo-3,5-difluorobenzene | HCID 136313 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3,5-Difluorophenyl)boronic acid | HCID 2734338 | — |
Reaction Steps
91.5 ml of tert-butyllithium are added at −78° C. to 20 g of 1-bromo-3,5-difluorobenzene in 300 ml of diethyl ether. The reaction mixture is stirred for 1 hour at −78° C. and 14.2 ml of trimethyl borate are then added. The reaction mixture is stirred for 1 hour at −78° C. and then for 12 hours at room temperature. 200 ml of aqueous 1 N hydrochloric acid solution are added. The resulting mixture is extracted with diethyl ether, the organic phase is washed with saturated sodium hydrogen carbonate solution and dried over magnesium sulphate, and the solvents are evaporated off under reduced pressure. The residue is taken up in cyclohexane and the precipitate obtained is isolated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482986B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-c6c23ebc83954ef28d4e6d0d5c14dda4 |
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| Source note | uspto-grants-2002_11 |
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