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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989254Generated: November 2, 2026

Triisopropyl borate → HCID 60209342, compound

https://huagongshe.com/reaction/1989254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantHCID 57468804HCID 57468804—
ReactantButyllithiumHCID 178418339—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 60209342HCID 60209342—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(3-bromo-phenyl)-4-methyl-6-(4-trifluoromethyl-phenyl)-pyridine (example E.90) (1.23 g, 3.13 mmol) in TBME (80 mL) at −78° C. was added n-BuLi (1.6 M in hexane, 3.2 mL, 5.0 mmol) keeping the internal temperature below −60° C. (ca. 3 min), stirring was continued at −78° C. for 25 min, then triisopropyl borate (1.5 mL, 6.27 mmol) was added quickly, causing the internal temperature to rise to −60° C., stirring was continued at −78° C. for 20 min. The mixture was quenched by addition of 1M NaH2PO4.2H2O-solution, the cooling bath was removed and the mixture was allowed to warm to 0° C. and stirred at 0° C. for 10 min. Diluted with EtOAc and brine, extracted three times with EtOAc, dried the combined organic layers over Na2SO4. Removal of the solvent in vacuum left the title compound as a light brown foam (1.20 g, 70.5%, purity: 65.8%), which was used without further purification. MS (ISP) 358.2 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-04f726213a8b48159f4d4b6269678326
Source noteuspto-grants-2010_01