HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757029Generated: October 28, 2026
Triisopropyl borate → 2-Octyloxy-5-pyridineboronic acid
https://huagongshe.com/reaction/1757029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 5-bromo-2-(octyloxy)Pyridine | HCID 14439231 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Octyloxy-5-pyridineboronic acid | HCID 22412798 | — |
Reaction Steps
2.75 g (10 mmol) of 2-octyloxy-5-bromopyridine are dissolved in 60 ml of absolute diethyl ether, and the solution is cooled to -75° C. under inert gas. 16 mmol of 1.6M butyllithium solution in hexane are added, and the mixture is additionally stirred at -75° C. for 15 minutes. 4.5 g of triisopropylborate in 50 ml of absolute diethyl ether are then added dropwise. The cooling device is then removed. After the batch has warmed to room temperature, 50 ml of 10% HCl are added, and the mixture is additionally stirred at room temperature for 30 minutes. The phases are separated, and the organic phase is washed twice with saturated NaCl solution. The solvent is distilled off in vacuo, and the residue is recrystallized from acetonitrile, giving 6-octyloxypyridine-3-boronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05443754 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-7291f1ffde824df6887bf39092a43130 |
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| Source note | uspto-grants-1995_08 |
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