Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-methyl-3-oxohept-6-enoateHCID 1095420558.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-395dad0db0ff437280a208c3408a9422
Source noteuspto-grants-2011_05