HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260906Generated: October 30, 2026
Hydrochloric Acid → 2,3-Difluoro-5-methylphenylboric acid
https://huagongshe.com/reaction/2260906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2,3-Difluorotoluene | HCID 2774228 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Product | 2,3-Difluoro-5-methylphenylboric acid | HCID 23118841 | — |
Reaction Steps
Under a nitrogen atmosphere, 30 g the compound (2) having been dissolved in 240 mL of THF was cooled to −78° C., to which 284 mL of sec-BuLi (1 M/L) was added, followed by stirring at the same temperature for 2 hours. 48.7 g of trimethyl borate having been dissolved in 120 mL of THF was added dropwise thereto at the same temperature, followed by stirring at the same temperature for 1 hour, and the mixture was increased in temperature to room temperature and then stirred over night. Under cooling with an ice bath, 200 mL of 3N hydrochloric acid was added to the mixture. The aqueous layer was extracted with diethyl ether, which was added to the organic layer, and the organic layer was washed with a saturated saline and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 48.8 g of 2,3-difluoro-5-methylphenylboric acid (3), which was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846513B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-c9212347386743b0a31c65a68a16ad30 |
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| Source note | uspto-grants-2010_12 |
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