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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458411Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 22100737, compound

https://huagongshe.com/reaction/1458411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22100801HCID 22100801—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22100737HCID 22100737—

Reaction Steps

To 2-methyl-5-(tert-butyldimethylsilyl)oxy-6-(N-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyanonaphth-1-yl)methylbenzimidazole (3 g) in THF (50 mL) was added tetrabutyl ammonium fluoride (3 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 and concentrated to afford 2-methyl-5-hydroxy-6-(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-5a9d39a4bd56464aafe95f7483271b88
Source noteuspto-grants-1998_12