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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989243Generated: October 30, 2026

Triisopropyl borate → HCID 57468822, compound

https://huagongshe.com/reaction/1989243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantHCID 57468823HCID 57468823—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57468822HCID 57468822—

Reaction Conditions

Temperature20 °C

Reaction Steps

Step 2) To a solution of the above prepared 4-bromo-2-(2,5-dimethyl-pyrrol-1-yl)-pyridine (1.95 g, 7.77 mmol) and triisopropyl borate (2.68 mL, 11.6 mmol) in THF (40 mL) at −78° C. was added n-BuLi (1.6 M in hexane, 4.85 mL, 7.77 mmol) keeping the internal temperature below −65° C. Stirring was continued at −78° C. for 1 h, then more triisopropyl borate (2.68 mL, 11.6 mmol) and n-BuLi (4.85 mL, 7.77 mmol) was added and stirring was continued at −78° C. for 1 h. The reaction mixture was quenched with 1 M NaH2PO4-sol., allowed to quickly (waterbath) warm to ca. 20° C. and stirred for 10 min. Diluted with EtOAc, layers were separated, washed organic layer with brine and dried over Na2SO4. Removal of the solvent in vacuum left the title compound as a yellow foam (2.1 g, 100%, 80% purity), which was used without further purification. MS (ISN) 215.3 [(M−H)−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-3c9fb7c98ad148c9ba6f5497fd80c1cc
Source noteuspto-grants-2010_01