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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant5-Bromo-2-hexyloxypyridineHCID 22118078—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product6-Hexyloxypyridine-3-boronic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022492
Source datasetuspto-grants-2000_02
ORD IDord-50185cdd3bd341b492f931a4b5d05d8c
Source noteuspto-grants-2000_02