HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789631Generated: October 31, 2026
Hydrochloric Acid → 4-ethoxy-2-trifluoromethylphenylboric Acid
https://huagongshe.com/reaction/1789631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-4-ethoxy-2-(trifluoromethyl)benzene | HCID 22034993 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-ethoxy-2-trifluoromethylphenylboric Acid | HCID 22035006 | 89.1% |
Reaction Steps
Compound (c) (10.0 g) dissolved in tetrahydrofuran (THF) (40 mL) was cooled to −78° C., a 1.6 M butyllithium/hexane solution (30 mL) was slowly added dropwise and the mixture was stirred at the same temperature for 2 hours. Triisopropyl borate (14.0 g) dissolved in THF (20 mL) was then slowly added dropwise at −78° C., and the mixture was stirred at the same temperature for 1 hour. The temperature was increased to room temperature and the final solution was stirred. After adding 3 M hydrochloric acid (200 mL) dropwise at ice-cooling temperature, the aqueous layer was extracted three times with ether. The organic layers were combined, washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 8.28 g of Compound (d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07070838B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-5820225fe8974a7692d95ff7a8e72a7a |
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| Source note | uspto-grants-2006_07 |
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