HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-Penten-3-yl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Pentene | HCID 8004 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Penten-3-yl Acetate | HCID 530323 | — |
Reaction Steps
The above pentene derivative (9.0 g, 25 mmols) and acetic anhydride (3.0 g, 30 mmols) are dissolved in ether (200 ml), followed by dropwise adding pyridine (5 ml), while stirring the solution under ice cooling, stirring the reaction liquid under ice cooling for one hour, elevating the temperature up to room temperature, stirring for 3 hours, pouring the reaction mixture into ice water after completion of the reaction, extracting with toluene (150 ml), washing the organic layer with water, drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 5-(4-(4-propylphenyl)phenyl)cyclohexyl)-3-acetyloxy-1-pentene pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05449810 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-3c3ae2aeb27a498d8f9b2159de3a625a |
| Source note | uspto-grants-1995_09 |