HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178442765, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Amino-4-(4-decylphenyl)phenol | HCID 19776123 | — |
| Reactant | HCID 178444542 | HCID 178444542 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178442765 | HCID 178442765 | 56.1% |
Reaction Steps
Step i) In a 50 ml-three-necked flask, 0.70 g (2.15 mM) of 2-amino-4-(4-decylphenyl)phenol, 0.48 g (2.21 mM) of trans-4-pentylcyclohexylcarbonyl chloride and 20 ml of dioxane were placed. To the mixture, 0.77 ml of pyridine was gradually added dropwise at about 87° C. under stirring, followed by heat-stirring for 1.5 hours at about 87° C. After the reaction, the reaction mixture was poured into 150 ml of water to precipitate a crystal. The crystal was recovered by filtration, washed with methanol and recrystallized from toluene to obtain 0.61 g of 2-(trans-4-pentylcyclohexylcarbonylamino)-4-(4-decylphenyl)phenol (yield: 56.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190690 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-9aab12bd6b014cd887c05cf29b84ad58 |
| Source note | uspto-grants-1993_03 |