HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330697Generated: October 26, 2026
Methyl acetoacetate → HCID 54125930, compound
https://huagongshe.com/reaction/330697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Hexa-2,4-dienal | HCID 8901 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54125930 | HCID 54125930 | 24.4% |
Reaction Steps
To a cold (-30° C.) solution of methyl acetoacetate (41.5 g, 357 mmol) in THF (500 mL) was added lithium diisopropylamide (476 mL, 1.5M solution in cyclohexane, 714 mmol). The resultant solution was stirred for 15 minutes at -30° C. After cooling to -78° C., 2,4-hexadienal (34.3 g, 357 mmol) was added and the solution stirred for 10 minutes at -78° C. and for 16 hours at ambient temperature. The solution was concentrated under reduced pressure and the residual syrup was partitioned between 1N HCl and ethyl acetate. The organic layer was washed with brine (2x), dried (Na2SO4), and concentrated. The residue was purified by chromatography on silica gel (diethyl ether:hexane/2:1) to afford 18.5 g (24.4%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04897490 |
|---|
| Source dataset | uspto-grants-1990_01 |
|---|
| ORD ID | ord-0946948dd89c419aa5a22e784bbfd428 |
|---|
| Source note | uspto-grants-1990_01 |
|---|