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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199168Generated: November 4, 2026

Methyl acetoacetate → Methyl 3-hydroxy-5-oxo-6,8-decadienoate

https://huagongshe.com/reaction/1199168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantHexa-2,4-dienalHCID 8901—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-hydroxy-5-oxo-6,8-decadienoateHCID 5412593024.4%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898950
Source datasetuspto-grants-1990_02
ORD IDord-c4d99814cdea45c0ab527e3ceceac0c5
Source noteuspto-grants-1990_02