HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221151Generated: October 25, 2026
Hydrochloric Acid → 3-(Difluoromethoxy)benzeneboronic acid
https://huagongshe.com/reaction/221151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | (Difluoromethoxy)benzene | HCID 68015 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Difluoromethoxy)benzeneboronic acid | HCID 17750069 | 57.6% |
Reaction Steps
A solution of 3-(difluoromethoxy)benzene (3.0 g) and triisopropoxyborane (2.78 g) in tetrahydrofuran (15 ml) was cooled to −78° C. under argon atmosphere, and thereto was added a solution of n-butyl lithium (1.59 M hexane solution, 9.3 ml). The mixture was stirred at same temperature for 10 minutes, warmed, and further stirred at room temperature overnight. Thereto was added 3N aqueous hydrochloric acid solution (10 ml), and the mixture was stirred at room temperature for 5 minutes. The mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was crystallized from hexane to give 3-difluoromethoxybenzeneboronic acid (1.6 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202984B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-226130e25f7740cabc95067854ef6488 |
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| Source note | uspto-grants-2012_06 |
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