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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252239Generated: October 29, 2026

Trimethyl borate → (6-Fluoropyridin-3-yl)boronic acid

https://huagongshe.com/reaction/2252239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant5-Bromo-2-fluoropyridineHCID 2783168—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(6-Fluoropyridin-3-yl)boronic acidHCID 2783397583.8%

Reaction Steps

To a mixture of 5-bromo-2-fluoro-pyridine (1.71 g, 6.20 mmol) in dry ether (100 mL) was added n-BuLi (1.6 M in hexane, 41.4 mL, 0.0663 mol) at −78° C. After 30 minutes, trimethyl borate (8.2 mL, 0.0722 mol) was added to the above mixture and the reaction was warmed to room temperature and stirred overnight. The reaction was quenched with water and brine and acidified with 10% HCl until pH=8. The mixture was extracted with EtOAc, washed with 50% brine, dried over MgSO4, filtered, concentrated to give 5.1 g (60%) of the desired product. The crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320986B2
Source datasetuspto-grants-2008_01
ORD IDord-389d1e60916a419da651bd801fcdf7e1
Source noteuspto-grants-2008_01