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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829806Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 10295484, compound

https://huagongshe.com/reaction/1829806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 10186857HCID 10186857—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10295484HCID 1029548462.3%

Reaction Steps

To an ice cooled solution of 1-[(2S,3R)-5-(6-bromo-2-naphthyloxy)-2-(tert-butyldimethylsilyloxy)-3-pentyl]imidazole-4-carboxamide (120 mg, 0.225 mmol) in THF (5 ml) was added dropwise 1.0 M tetra-n-butylammonium fluoride in THF (338 μl). After the addition was completed, the reaction mixture was stirred at ice-bath temperature for 2 hours. The reaction was quenched by addition of 25% aqueous AcONH4 (5 ml) and H2O (10 ml) The resulting mixture was stirred for several minutes and then extracted with ethyl acetate (30 ml). The organic layer was washed with brine, dried (sodium sulfate) and concentrated under reduced pressure. The residue was purified by silica gel (4 g) column chromatography eluting with chloroform/methanol (100:1 to 20:1) to give 1-[(2S,3R)-5-(6-bromo-2-naphthyloxy)-2-hydroxy-3-pentyl]imidazole-4-carboxamide (16) (58.6 mg, 62.2%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064144B2
Source datasetuspto-grants-2006_06
ORD IDord-867abbd730bb4ff8983a4c6a90dc1bf8
Source noteuspto-grants-2006_06