Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455198Generated: November 2, 2026

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

https://huagongshe.com/reaction/1455198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorateHCID 26574—
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 triisoporpyl 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 acatate 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 numberUS07482366B2
Source datasetuspto-grants-2009_01
ORD IDord-7c39fe0fee874e0f8b4785453007688d
Source noteuspto-grants-2009_01