HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857563Generated: November 2, 2026
Iodine → 2-(Benzyloxy)-4-methoxyphenylboronic acid
https://huagongshe.com/reaction/1857563
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Bromo-4-methoxy-2-phenylmethoxybenzene | HCID 18434029 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | 2-(Benzyloxy)-4-methoxyphenylboronic acid | HCID 11832085 | — |
Reaction Steps
To a stirred and gently refluxing suspension of magnesium powder (382 mg, 15.7 mmol) in THF (10 ml) containing a few crystals of iodine, was added dropwise, a solution of 2-benzyloxy-1-bromo-4-methoxybenzene (WO 93/08799, 4.39 g, 15.0 mmol) in THF (40 ml). After completion of the addition, the mixture was refluxed for 1.25 hours, cooled and then transferred via a canula to a stirred solution of trimethyl borate (3.11 g, 3.40 ml, 30.0 mmol) in THF (25 ml) at -78° C. The mixture was stirred at -78° C. for 30 minutes and then the cooling bath was removed and stirring was continued at room temperature for a further 2 hours. The mixture was partitioned between diethyl ether and 1 N HCl (200 ml) and the product was extracted into diethyl ether. The extracts were washed with water, dried (MgSO4) and concentrated to give a yellow solid. Trituration with warm diethyl ether/n-hexane gave after drying the title compound as a cream solid. Yield 2.159 g (56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147111 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-7be2ef9c3b7d46b79bcfb185e1f89334 |
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| Source note | uspto-grants-2000_11 |
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