HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566161Generated: October 30, 2026
Hydrochloric Acid → HCID 18373957, compound
https://huagongshe.com/reaction/566161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 18373957 | HCID 18373957 | 69.3% |
Reaction Steps
To a mixture of 1-bromo-4-ethylbenzene (743 mmol) and 500 ml of THF, was added dropwise 500 ml of a solution of n-butyl lithium (corresponding to 780 mmol) in hexane at −78° C. in 1.6 hours, and stirred at the same temperature for 1.5 hours. To this solution was added dropwise 200 ml of a solution of triisopropyl borate (1,486 mmol) in THF, the solution was gradually warmed up to room temperature, and then the solution was stirred overnight. After 750 ml of 7.3% hydrochloric acid was added and stirred for 30 min, the reaction solution was extracted twice with diethyl ether, washed thrice with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was recrystallized from about 1,000 ml of toluene to give a white solid of 4-ethylphenyl boric acid (515 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174458B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-0515dfe68f7741cdaafe58fa44c1c1c9 |
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| Source note | uspto-grants-2001_01 |
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