Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349286Generated: October 30, 2026

Acetic Acid → [1-(3,5-Bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-(3-phenyl-3H-[1,2,3]triazol-4-yl)-methanone

https://huagongshe.com/reaction/349286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantt-Butylammonium fluorideHCID 21866379—
Reactant[1-(3,5-Bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-(3-phenyl-5-trimethylsilanyl-3H-[1,2,3]triazol-4-yl)-methanoneHCID 86601239—
SolventTetrahydrofuranHCID 8028—
Product[1-(3,5-Bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-(3-phenyl-3H-[1,2,3]triazol-4-yl)-methanoneHCID 58804034—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of [1-(3,5-Bis-trifluoromethyl-benzyl)-5-phenyl-1H-[1,2,3]triazol-4-yl]-(3-phenyl-5-trimethylsilanyl-3H-[1,2,3]triazol-4-yl)-methanone (0.050 g, 0.08 mmol) in THF (2 mL) add t-butyl ammonium flouride (1 M soln. in THF, 1.2 mL, 1.2 mmol) and acetic acid (120 μL, 2.0 mmol) and heat at 65° C. After 72 h., remove from heat, and quench with sat. aq. NH4C1 and H2O. Extract with EtOAc, dry over MgSO4, filter, and purify by flash chromatography (EtOAc/Hexane 0%–50%) to give the title compound. 1H NMR (300 MHz, CDCl3) δ 8.88 (s, 1H), 7.75 (s, 1H), 7.57–7.29 (m, 10H), 7.09 (m, 2H), 5.50 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179804B2
Source datasetuspto-grants-2007_02
ORD IDord-6a3f7472d5324174ba00cac6ebc6f7c2
Source noteuspto-grants-2007_02