HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (E,E)-1-acetoxy-4-ethyl-2,4-heptadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (E,E)-4-ethyl-2,4-heptadien-1-ol | HCID 86749298 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (E,E)-1-acetoxy-4-ethyl-2,4-heptadiene | HCID 86749299 | 74.3% |
Reaction Steps
To a solution of (E,E)-4-ethyl-2,4-heptadien-1-ol (10.1 g) in pyridine (29 g) at 0° C. was added dropwise acetic anhydride (22.2 g). After two hours at room temperature, the reaction mixture was evaporated in vacuo. The residue was diluted with ethyl acetate, washed with 0.5N hydrochloric acid and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (5% ethyl acetate in hexane) to give (E,E)-1-acetoxy-4-ethyl-2,4-heptadiene (9.75 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05495023 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-4533bf6cd86448a4b3bb372bb1d98a34 |
| Source note | uspto-grants-1996_02 |