HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584302Generated: October 30, 2026
Hydrochloric Acid → (5-(Ethoxymethoxy)-2-ethylphenyl)boronic acid
https://huagongshe.com/reaction/584302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-2-ethyl-5-ethoxymethoxybenzene | HCID 22345616 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (5-(Ethoxymethoxy)-2-ethylphenyl)boronic acid | HCID 22345587 | — |
Reaction Steps
12 g (49 mmol) of 1-bromo-2-ethyl-5-ethoxymethoxybenzene are placed in 200 ml of dry THF in a round-bottomed flask and under a stream of nitrogen. The reaction medium is cooled to −78° C. and 23 ml (58 mmol) of 2.5M n-butyllithium in hexane are added dropwise. 20 minutes later, 13.6 ml (59 mmol) of triisopropyl borate are added slowly. Stirring is continued for 1 hour at −78° C. The mixture is then poured into a solution of water and hydrochloric acid and is then extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a mixture of heptane and ethyl acetate (50/50). After evaporating off the solvents, 6.7 g (65%) of the expected product are obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924400B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-d6fd86ff902941e38ed4258c2270b3d2 |
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| Source note | uspto-grants-2005_08 |
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