HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604603Generated: October 25, 2026
Trimethyl borate → 5-(tert-Butyl)-2-methoxybenzeneboronic acid
https://huagongshe.com/reaction/604603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 4-Tert-butyl-2-iodo-1-methoxybenzene | HCID 14914462 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(tert-Butyl)-2-methoxybenzeneboronic acid | HCID 14740579 | — |
Reaction Steps
To a solution of 4-tert-butyl-2-iodo-1-methoxybenzene (0.164 g, 0.56 mmol) in dry THF (5 mL) at −78° C., n-butyl lithium (0.27 mL, 0.68 mmol, 2.5 M) was added. The solution was stirred at −78° C. for 30 min. Trimethyl borate (0.19 mL, 1.70 mmol) was added. The solution was stirred at −78° C. for 3 h. The reaction was quenched with saturated aqueous NH4Cl. The aqueous layer was extracted with EtOAc (3×15 mL). The combined EtOAc layers were dried over Na2SO4. The residue was used without further purification after evaporation of the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-dfe5c271b00d45bc8ac467ae3c6fd1e8 |
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| Source note | uspto-grants-2011_03 |
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