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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906831Generated: October 30, 2026

Triisopropyl borate → (6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid

https://huagongshe.com/reaction/906831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant5-Bromo-2-ethoxy-3-(trifluoromethyl)pyridineHCID 67389975—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acidHCID 6738938778.6%

Reaction Steps

Alternatively, n-butyl lithium (1.6 M solution in hexane, 0.9 mL, 1.43 mmol) was slowly added to a solution of 5-bromo-2-ethoxy-3-trifluoromethyl-pyridine (352 mg, 1.3 mmol) in 2.6 mL anhydrous Et2O at −78° C. under nitrogen. The mixture was kept at −78° C. for 1 hr, and then to this mixture was added triisopropyl borate (489 mg, 2.6 mmol). The mixture was allowed to warm to ambient temperature overnight. The reaction was quenched by water and the pH was adjusted to 5 by carefully addition of 1N aqueous HCl. Two layers were separated and the aqueous layer was extracted with ethyl acetate three times. The extract was washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 2-ethoxy-3-trifluoromethylpyridine-5-boronic acid as a brown oil (240 mg, 67% yield). The product was used for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013001B2
Source datasetuspto-grants-2011_09
ORD IDord-69c985d4c4834cda9958efe2d5ac9a5a
Source noteuspto-grants-2011_09