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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253384Generated: November 1, 2026

Triethyl borate → HCID 23080943, compound

https://huagongshe.com/reaction/2253384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl borateHCID 9009—
ReactantAmmonium ChlorideHCID 25517—
Reactant3,5-Dimethoxybenzyl alcoholHCID 69718—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23080943HCID 23080943—

Reaction Steps

To a solution of 3,5-dimethoxybenzyl alcohol (2.71 g) in tetrahydrofuran (50 mL) was added n-butyllithium (1.56M hexane solution; 36.2 mL)while cooling with ice with ice bath, and the internal temperature was raised to room temperature and stirred for 1 hour. The internal temperature was then cooled to −78° C., to the mixture was added triethoxyborane (9.6 mL), and the temperature was raised to room temperature while stirring. After completion of the reaction, saturated aqueous ammonium chloride was added to the reaction mixture while cooling with ice and the reaction mixture was extracted with ethyl acetate, and then after washing the organic extract with brine, it was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (50 g) and the title compound (1.72 g) was obtained as a white amorphous solid from the ethyl acetate fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-41d333fc25304e139e95980ff0a3b9f6
Source noteuspto-grants-2008_01