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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81494Generated: October 25, 2026

Hydrochloric Acid → [5-(Trifluoromethyl)pyridin-3-yl]boronic acid

https://huagongshe.com/reaction/81494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethyl borateHCID 9009—
Reactant3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
ReactantIsohexane ethyl acetateHCID 21882781—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[5-(Trifluoromethyl)pyridin-3-yl]boronic acidHCID 45158900—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Triethylborate (24 ml, 139 mmol) is added to a solution of 3-bromo-5-trifluoromethyl-pyridine (30 g, 133 mmol) in THF (300 ml) and the resulting pale yellow solution is cooled to −78° C. A solution of 1.6 M n-butyl lithium in hexanes (97 ml, 139 mmol) is added via cannula dropwise over 40 minutes, keeping the temperature below −65° C. Once addition is complete, the reaction mixture is allowed to warm slowly to room temperature and stirred for 1 hour. 1M HCl (200 ml) is added and the reaction mixture stirred for 15 minutes. The layers are separated and the organic layer is washed with 1M HCl (200 ml). The aqueous layers are combined and washed with EtOAc (2×250 ml). The pH of the aqueous phase is adjusted by the addition of 2M NaOH, and extracted with EtOAc (2×250 ml). Concentration in vacuo affords a solid, which is recyrstallised from EtOAc/iso-hexane to yield the title compound as a yellow solid [M+H]+ 192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846687B2
Source datasetuspto-grants-2014_09
ORD IDord-50ae31e39c944dd8a487edfe853fb192
Source noteuspto-grants-2014_09