HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341681Generated: October 26, 2026
Hydrochloric Acid → 4'-Chloro-3-methylbiphen-4-ylboronic acid
https://huagongshe.com/reaction/341681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 4-Bromo-4'-chloro-3-methylbiphenyl | HCID 59450516 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Chloro-3-methylbiphen-4-ylboronic acid | HCID 59450493 | 59.4% |
Reaction Steps
n-Butyl lithium (1.6 M solution in hexanes, 37.5 ml, 0.060 mol) is added dropwise to a solution of 4-bromo-4′-chloro-3-methylbiphenyl (11.5 g, 0.041 mol) in tetrahydrofuran (120 ml) at −78° C., under an atmosphere of nitrogen, and the mixture is stirred at −78° C. for 30 minutes. Trimethyl borate (27.4 ml, 0.245 mol) is added slowly at −78° C. and the mixture is stirred for 1 hr. The reaction mixture is allowed to warm to room temperature over 2-3 hours and then stirred at room temperature for 1 hr. 0.1N Aqueous hydrochloric acid (320 ml) is added and the mixture is stirred at room temperature overnight. The reaction mixture is extracted with ethyl acetate (3×300 ml) and the organic extracts are combined, dried with anhydrous sodium sulfate, filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4′-chloro-3-methylbiphen-4-ylboronic acid (6.0 g) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895761B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f8491472caa346e185240b41242fb8b2 |
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| Source note | uspto-grants-2014_11 |
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