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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937120Generated: November 3, 2026

Methyl triflate → HCID 22463489, compound

https://huagongshe.com/reaction/1937120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl triflateHCID 9526—
Reactantalpha-HydroxyacetophenoneHCID 68490—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventNitromethaneHCID 6375—
ProductHCID 22463489HCID 22463489—

Reaction Steps

Methyltriflate (1 mL, 8.84 mmol) was added dropwise to a solution of (0.959 g, 5.92 mmol) carbonyl diimidazole dissolved in 20 ml nitromethane. The solution was kept at about 0° C. during the addition. The solution was then warmed to room temperature and was allowed to stir for 1 h. The solution was then transferred to a flask containing freshly azeotroped (from benzene) 0.647 g (5.303 mmol) phenacyl alcohol. The resulting mixture was allowed to stir for 2 h at room temperature to form the phenacyl carbonyl-N-methylimidazole (not isolated or characterized). Freshly azotroped isopropyl alcohol (5.92 mmol) was then added and the reaction mixture was stirred overnight. The solvent was removed by vacuum distillation and the product was purified using silica gel flash chromatography with 80% hexane and 20% ethyl acetate. Yield 1.032 g (88%) from 0.715 g phenacyl alcohol, yellow oil; 1H NMR (CDCl3, 400 MHz) δ3.87 (s, 3H), 5.37 (s, 2H), 7.46-7.62 (m, 3H), 7.92 (d, J=6, 2H); 13C NMR (CDCl3, 110 MHz) δ191.9, 154.2, 133.8, 128.7, 127.5, 72.6, 68.2, 21.5; EI-MS, m/z (rel. intensity) 222 (M+, 1), 163 (27), 118 (32), 105 (100), 91 (60), 77 (66), 65 (13), 50 (44).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06392089B1
Source datasetuspto-grants-2002_05
ORD IDord-4edb99aa8121475a8344aa74fd81189d
Source noteuspto-grants-2002_05