HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoro-4-nitrophenol → 6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoro-4-nitrophenol | HCID 520948 | — |
| Reactant | 4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline | HCID 22646522 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinoline | HCID 22936573 | 62.5% |
Reaction Steps
4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (1.7 g) and 3-fluoro-4-nitrophenol (2.0 g) were suspended in chlorobenzene (20 ml), and the suspension was heated to reflux for 6 hours. After completion of the reaction, the solvent was distilled off, ethyl acetate was added, and a solid precipitated. The solid was filtered out and washed with ether, washed with 1N sodium hydroxide water and with water, and then dried to obtain 1.55 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372981B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-e45c9bc7abb24bbd8e51f63f71fd3892 |
| Source note | uspto-grants-2013_02 |