HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(4-Decyloxybenzoylamino)-4-octylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Phenol, 2-amino-4-octyl- | HCID 87767 | — |
| Reactant | 4-Decyloxybenzoyl chloride | HCID 11779353 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Decyloxybenzoylamino)-4-octylphenol | HCID 19021154 | 97.4% |
Reaction Steps
In a 50 ml-three-necked flask, 0.50 g (2.43 mM) of 2-amino-4-octylphenol, 0.82 g (2.54 mM) of 4-decyloxybenzoyl chloride and 20 ml of dioxane were placed and heated. To the mixture, 0.88 ml of pyridine was gradually added dropwise at around 90° C. under stirring, followed by further stirring for 35 minutes at around 90° C. After the reaction, the reaction mixture was poured into water to precipitate a crystal. The crystal was recovered by filtration and washed with water, followed by recrystallization from hydrous acetone to obtain 1.06 g of 2-(4-decyloxybenzoylamino)-4-octylphenol (yield: 90.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05318720 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-0d3bac9c0abb4c559257239174c483bd |
| Source note | uspto-grants-1994_06 |