HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Phenyl nicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Nicotinoyl chloride | HCID 82604 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl nicotinate | HCID 77018 | — |
Reaction Steps
Nicotinic chloride (1.78 g, 10 mmoL) was added to phenol (1.29 g, 12 mmoL) in 10 mL of tetrahydrofuran (THF). Triethylamine (5 mL) and pyridine (5 mL) were then added to the mixture, which was then stirred at room temperature overnight. After THF was evaporated, the mixture was washed with ethyl acetate in water for three times. The ethyl acetate (EtOAC) layer was then purified with silica column (Hexane: EtOAC=4:1) to give pure product. 1H NMR (400 MHz, CDCl3): δ=9.40 (s, 1H), 8.86 (d, 1H), 8.46 (d, 1H), 7.45 (m, 3H), 7.32 (d, 1H), 7.24 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321797B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-9265f1ae3eaa42f38f4dd493ee9f13f2 |
| Source note | uspto-grants-2016_04 |