Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant5-bromo-2-(octyloxy)PyridineHCID 14439231—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product2-Octyloxy-5-pyridineboronic acidHCID 22412798—

Reaction Conditions

Temperature-75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05443754
Source datasetuspto-grants-1995_08
ORD IDord-7291f1ffde824df6887bf39092a43130
Source noteuspto-grants-1995_08