HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Fluoro-3-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Chloro-3-nitrobenzaldehyde | HCID 85505 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Fluoro-3-nitrobenzaldehyde | HCID 598129 | 98.2% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
93 g (0.5 mol) of 4-chloro-3-nitrobenzaldehyde and 58 g (1 mol) of potassium fluoride are suspended in 250 mol of dimethylformamide. The reaction mixture contains 0.02% of H2O. The mixture is stirred for one hour at 160° C. and the dimethylformamide is evaporated off in vacuo. The residue is cooled and stirred with 200 ml of water, the mixture is extracted with methylene chloride and the organic phase is dried. After the methylene chloride has been evaporated off, 83 g of 4-fluoro-3-nitrobenzaldehyde with a content of 90.2% are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04456772 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-12465fbdb8a34f8696f5542a5ab32848 |
| Source note | uspto-grants-1984_06 |