HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluoronitrobenzene → Methyl 2-(1-methylpyrrol-2-yl)-2-(4-nitrophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 1-methylpyrrol-2-acetate | HCID 103992 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(1-methylpyrrol-2-yl)-2-(4-nitrophenyl)acetate | HCID 23285895 | 97% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methyl 1-methylpyrrole-2-acetate (5.32 g, 34.73 mmol) and 4-fluoro-nitrobenzene (4.9 g, 34.73 mmol) were dissolved in dry DMF (100 ml), and the solution was cooled to 0° C. under nitrogen. Sodium hydride powder (1.75 g, 72.93 mmol) was added in portions. After 30 min the reaction mixture was quenched with 1 M HCl and the product was extracted into ether. The organic extracts were washed with water and brine, and dried over magnesium sulfate. The solvent was removed in vacuo to give methyl-2-(1-methylpyrrol-2-yl)-2-(4-nitrophenyl)acetate (9.20 g, 97%) as a red oil. ##STR61##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127402 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-b6b5761c5ea1477bba005406e721c3ac |
| Source note | uspto-grants-2000_10 |