HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376753Generated: October 26, 2026
Hydrochloric Acid → 6-Hexyloxypyridine-3-boronic acid
https://huagongshe.com/reaction/376753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 5-Bromo-2-hexyloxypyridine | HCID 22118078 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Hexyloxypyridine-3-boronic acid | HCID 22112571 | — |
Reaction Steps
250 mmol of n-butyllithium (1.6M solution in n-hexane) are added dropwise at 0° C. with exclusion of moisture and under a protective-gas atmosphere to a solution of 250 mmol of 5bromo-2-hexyloxypyridine in 500 ml of abs. diethyl ether. The mixture is stirred at this temperature for a further 1 hour, and 275 mmol of trimethyl borate are subsequently added slowly. After the mixture has been stirred at 0° C. for a further hour, a solution of 175 ml of water and 25 ml of 37 percent hydrochloric acid is added dropwise. The mixture is stirred at room temperature for 1 hour, the phases are then separated, the aqueous phase is extracted a number of times with dichloromethane, and the combined organic extracts are dried using magnesium sulfate. The solvents are removed in vacuo. After drying in a high vacuum, the red-brown, high-viscosity crude product is reacted further without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022492 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-50185cdd3bd341b492f931a4b5d05d8c |
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| Source note | uspto-grants-2000_02 |
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