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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330654Generated: October 30, 2026

Ethyl Acetoacetate → Ethyl 9,9-bis(4-fluorophenyl)-5-hydroxy-8-(1-ethyl-1H-tetrazol-5-yl)-3-oxo-6,8-nonadienoate

https://huagongshe.com/reaction/330654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
Reactant5,5-bis(4-fluorophenyl)-4-(1-ethyl-1H-tetrazol-5-yl)2,4-pentadienalHCID 54555804—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 9,9-bis(4-fluorophenyl)-5-hydroxy-8-(1-ethyl-1H-tetrazol-5-yl)-3-oxo-6,8-nonadienoateHCID 86743727—

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of 0.5 g (1.4 mmoles) of 5,5-bis(4-fluorophenyl)-4-(1-ethyl-1H-tetrazol-5-yl)2,4-pentadienal in tetrahydrofuran at -50° C., was added 1.75 mL of 0.8M (1.4 mmoles) of a freshly prepared solution of ethyl acetoacetate dianion [described in Example 10]. The solution was stirred for 30 minutes at -50° C. and then allowed to warm to -10° C. during the next 30 minutes. The solution was quenched with 1N HCl and extracted with methylene chloride. The organic extracts were dried and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with chloroform to give 0.4 g of the title compound as an oil. MS (CI): m/e=497 for (M+H)+ ;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897490
Source datasetuspto-grants-1990_01
ORD IDord-1e526294427c44829d3c9a79c6068a42
Source noteuspto-grants-1990_01