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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458413Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 22100711, compound

https://huagongshe.com/reaction/1458413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22100652HCID 22100652—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22100711HCID 22100711—

Reaction Steps

To 2-methyl-6-(tert-butyldimethylsilyl)oxy-5-(N-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyanonaphth-1-yl)methylbenzimidazole (3 g) in THF (50 mL) was added Bu4NF (4 mL, 1M)) at ambient temperature. After stirring at ambient temperature for 30 minutes the solvent was removed. The reaction was worked up between ethyl acetate and H2O. The organic layer was dried, concentrated and purified by silica gel chromatography (hexane/ethyl acetate/CH2Cl2 /methanol, gradient) to afford 2-methyl-6-hydroxy-5-(N-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyanonaphth-1-yl)methylbenzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849759
Source datasetuspto-grants-1998_12
ORD IDord-ed1d1ab9692a4748a9c2748a6c4eb89d
Source noteuspto-grants-1998_12