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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195358Generated: October 31, 2026

Ethyl Acetoacetate → HCID 54092866, compound

https://huagongshe.com/reaction/1195358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantHCID 53801859HCID 53801859—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54092866HCID 54092866—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl acetoacetate dianion (2.6 mL of a freshly prepared 1M solution as described in Example 10) was added to a solution of 5,5-bis(4-fluorophenyl)-4-[1-(2-methoxyethoxy)methyl-1H-tetrazol-5-yl]-2,4-pentadienal (1.1 g, 2.6 mmoles) in 15 mL of tetrahydrofuran at -40° C. After stirring for 2 hours, analytical TLC eluted with 25% (v/v) ethyl acetate in hexane showed starting aldehyde and therefore, another 1.2 mL of dianion solution was added. The reaction mixture was allowed to warm to 0° C. and then quenched with 1N HCl. The mixture was extracted with methylene chloride, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with 1% (v/v) methanol in methylene chloride to give 0.9 g of the title compound as an oil. MS (CI): m/e=557 for (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110940
Source datasetuspto-grants-1992_05
ORD IDord-4164c0d039be421d967ea324a50aa08d
Source noteuspto-grants-1992_05