HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566154Generated: October 30, 2026
Hydrochloric Acid → 4-(4-Methoxymethylcyclohexyl) phenyl boric acid
https://huagongshe.com/reaction/566154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 4-(4-Methoxymethylcyclohexyl)-1-iodobenzene | HCID 13742649 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(4-Methoxymethylcyclohexyl) phenyl boric acid | HCID 23297291 | 20.2% |
Reaction Steps
To a mixture of 4-(4-methoxymethylcyclohexyl)-1-iodobenzene (297 mmol) and 250 ml of THF, was added dropwise 200 ml of a solution of n-butyl lithium (corresponding to 312 mmol) in hexane at −78° C. in 3.0 hours, and stirred at the same temperature for 1.2 hours. To the solution was added dropwise 100 ml of a solution of triisopropyl borate (594 mmol) in THF, the solution was gradually warmed up to room temperature, and then the solution was stirred overnight. After 270 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 dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was washed with heptane to give a white solid of 4-(4-methoxymethylcyclohexyl) phenyl boric acid (60.1 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-c94d19fb7a934133a866d8ea8565273f |
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| Source note | uspto-grants-2001_01 |
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