HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (E,E)-4-ethyl-2,4-heptadien-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | methyl (E,E)-4-ethyl-2,4-heptadienoate | HCID 12700325 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (E,E)-4-ethyl-2,4-heptadien-1-ol | HCID 86749298 | 91.8% |
Reaction Steps
To a suspension of lithium aluminum hydride (2.38 g) in ethyl ether (160 ml) was added a solution of methyl (E,E)-4-ethyl-2,4-heptadienoate (13.2 g) in ethyl ether (100 ml) while keeping the temperature below 30° C. When addition was completed, the mixture was allowed to stir at room temperature for one hour. To this resultant mixture at 10° C. were added dropwise ethyl acetate (50 ml) and a saturated aqueous solution of potassium sodium tartrate (50 ml). The separated organic layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated to give (E,E)-4-ethyl-2,4-heptadien-1-ol (10.1 g) as an oil. This oil was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05691366 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-a41689ec10c54254ac86f6231480ddff |
| Source note | uspto-grants-1997_11 |