HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551665Generated: October 31, 2026
Ethyl 2-methylacetoacetate → Ethyl 2-methyl-3-oxohept-6-enoate
https://huagongshe.com/reaction/551665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-methyl-3-oxohept-6-enoate | HCID 10954205 | 58.9% |
Reaction Steps
Ethyl 2-methyl-3-oxobutanoate (10 mL, 70.7 mmol) was added dropwise to an anhydrous tetrahydrofuran suspension of sodium hydride (2.83 g, 74.2 mmol) with stirring under ice cooling. The mixture was stirred for 15 minutes in this bath. Then, n-butyllithium (1.59 M hexane solution, 45.3 mL, 72.1 mmol) was added dropwise thereto, and the mixture was further stirred for 30 minutes. Then, allyl bromide (6.73 mL, 77.7 mmol) was added dropwise thereto. After removal of the ice bath, the mixture was stirred for 2 hours, and the reaction was then terminated by pouring dilute hydrochloric acid to the reaction solution. The reaction solution was subjected to extraction with ethyl acetate. The organic layer was washed with water, saturated aqueous sodium bicarbonate, and saturated saline and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain the compound of interest as a pale yellow oil (7.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07947738B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-395dad0db0ff437280a208c3408a9422 |
|---|
| Source note | uspto-grants-2011_05 |
|---|