HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrofungin → 2-Chloro-5-(2-chloro-4-nitrophenoxy)methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrofungin | HCID 12074 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(Bromomethyl)-2-chloropyridine | HCID 6424661 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-5-(2-chloro-4-nitrophenoxy)methylpyridine | HCID 20537903 | — |
Reaction Steps
2-Chloro-4-nitrophenol (17.4 mmol) in 15 ml of THF is slowly added to a stirring suspension of sodium hydride (17.4 mmol) in 25 ml of THF. After gas evolution has ceased, 2-chloro-5-bromomethylpyridine is added and the mixture is heated under reflux overnight. The reaction is diluted with water, extracted with chloroform, washed with water, dried and stripped to give 2-chloro-5-(2-chloro-4-nitrophenoxy)methylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04332944 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-9d88b87fcce641edb3c7de8afa9f3ca0 |
| Source note | uspto-grants-1982_06 |