HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → bis(4-Fluorophenyl)methyl(5-formyl-1H-1,2,4-triazol-1-ylmethyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Flusilazole | HCID 73675 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | bis(4-Fluorophenyl)methyl(5-formyl-1H-1,2,4-triazol-1-ylmethyl)silane | HCID 14154941 | 80.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Bis(4-fluorophenyl)methyl(1H-1,2,4-triazol-1-ylmethyl)silane (1.3 g, 0.004 mol) was lithiated as described in Example 1 using 3.7 mL (0.0044 mol) of 1.2M n-butyllithium in 10 mL of THF. DMF (1.2 mL, 0.016 mol) was added and the solution was allowed to warm to 0° C. After 1 hour, the reaction mixture was diluted with 1:1 ether/hexanes, washed with 7% aqueous NaHCO3 and brine, dried over Na2SO4 and evaporated. Flash chromatography using 10% ether/methylene chloride gave 1.1 g of the title compound as a clear oil: nD 1.5612; ir (neat) 2840, 1705, 1587, 1499, 1228, 1160, 1106, 821 cm-1 ; nmr (CDCl3) δ, 0.7 (3H, s), 4.7 (2H, s), 7.0 (4H, t), 7.4 (4H, m), 7.9 (1H, s), 9.8 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04729986 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-a4502ca3359746bba29aea7ceee88041 |
| Source note | uspto-grants-1988_03 |