Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748651Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 69206630, compound

https://huagongshe.com/reaction/748651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 59751486HCID 59751486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69206630HCID 69206630—

Reaction Steps

2-(tert-butyl-dimethyl-silanyl)-4-(hydroxy-thiophen-2-yl-methyl)-imidazole-1-sulfonic acid dimethylamide (Intermediate-E1) (2.5 g, 6.2 mmol) in THF (60 mL) was treated with tetrabutylammonium fluoride (TBAF) (6.9 mL of a 1M soln) at 0° C. for 1 h and at rt for 3 h. The reaction mixture was subjected to an aqueous work-up and the product was purified by chromatography on silica gel with EtOAc to give 4-(hydroxy-thiophen-2-yl-methyl)-imidazole-1-sulfonic acid dimethylamide as a white solid, 1.43 g. 4-(Hydroxy-thiophen-2-yl-methyl)-imidazole-1-sulfonic acid dimethylamide (0.5 g, 1.74 mmol) in dichloromethane (25 mL) was reacted with trifluoroacetic acid (4.3 mL, 56 mmol) and triethylsilane (TES) (2.2 mL, 14 mmol) at rt for 18 h. The mixture was quenched with water and solid NaHCO3. This material was subjected to an aqueous work-up and the residue was purified by chromatography on silica gel with 50% EtOAc: hexane to yield 4-thiophen-2-ylmethyl-imidazole-1-sulfonic acid dimethylamide (Intermediate-E2) 0.44 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399868B2
Source datasetuspto-grants-2008_07
ORD IDord-92467fe03f6b4dcc8d9e593a6154ea8c
Source noteuspto-grants-2008_07