HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-Butyroylamino-4-(4-nitrophenoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 4-(4-Nitrophenoxy)pyridin-2-amine | HCID 22936716 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Butyroylamino-4-(4-nitrophenoxy)pyridine | HCID 22936677 | — |
Reaction Steps
Butyroyl chloride (0.93 ml) was added dropwise to a stirred solution of 2-amino-4-(4-nitrophenoxy)pyridine (1.0 g), triethylamine (1.8 ml) and tetrahydrofuran (20 ml) at room temperature. After stirring for 1 hour, water was added, extraction was performed with ethyl acetate, the extract was dried over magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=2:1) to obtain 0.6 g of the target substance as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372981B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-9fa824a0ae0747188954ececcfc9e181 |
| Source note | uspto-grants-2013_02 |