HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587282Generated: October 29, 2026
N-Methoxy-N-methylacetamide → 1-(1-(4-vinylphenyl)-1H-1,2,4-triazol-5-yl)ethanone
https://huagongshe.com/reaction/587282
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | 1-(4-vinylphenyl)-1H-1,2,4-triazole | HCID 58549964 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-(4-vinylphenyl)-1H-1,2,4-triazol-5-yl)ethanone | HCID 86675219 | — |
Reaction Steps
To a stirred solution of 1-(4-vinyl-phenyl)-1H-[1,2,4]triazole (1 g, 5.8 mmol) in 25 mL of THF, was added n-BuLi (0.37 g, 5.8 mmol) at −78° C. and stirred for 30 min To this N-methoxy-N-methyl acetamide in THF (0.66 g, 6.4 mmol) was added and the resultant reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was quenched with a saturated aqueous NH4Cl solution and extracted with EtOAc (3×50 mL). The combined EtOAc layer was washed with brine and dried over sodium sulphate and concentrated under reduced pressure. The crude compound was purified by flash chromatography (SiO2, 100-200 mesh, 40% EtOAc in Pet ether) to afford the title compound as an off white solid (280 mg, 23%): mp 97-98° C.; 1H NMR (400 MHz, CDCl3) δ 8.10 (s, 1H), 7.50 (d, 2H), 7.38 (d, 2H), 6.68 (dd, 1H), 5.85 (d, 1H), 5.38 (d, 1H), 2.75 (s, 3H); ESIMS m/z 214.14 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226500B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-f570ccd375684b3ca262a58444a5e034 |
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| Source note | uspto-grants-2016_01 |
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