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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330675Generated: October 29, 2026

Tert-butyl acetoacetate → HCID 54272216, compound

https://huagongshe.com/reaction/330675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl acetoacetateHCID 15538—
ReactantSodium hydrideHCID 24758—
ReactantHCID 53912652HCID 53912652—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54272216HCID 54272216—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 5,5-bis(4-fluoro-2-methylphenyl)-4-(1-methyl-1H-tetrazol-5-yl)-2,4-pentadienal (1.0 g, 2.5 mmoles) in tetrahydrofuran at -50° C. was added the dianion of t-butyl acetoacetate (2.5 mL of a 1M solution, 2.5 mmoles) prepared by adding t-butyl acetoacetate (4.0 g, 25.0 mmoles) in tetrahydrofuran (4 mL) to a suspension of sodium hydride (1.0 g of 60% dispersion, 25.0 mmoles) in tetrahydrofuran at -5° C. followed by cooling to -30° C. and the addition of butyl lithium (11.4 mL of 2.2M solution, 25 mmoles). After stirring for 1.5 hours, analytical TLC indicated starting aldehyde and another 0.5 mL of dianion solution was added. The solution was stirred an additional 0.5 hour and quenched with 1N hydrochloric acid. The mixture was extracted with methylene chloride. The extracts were dried and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with methanol in methylene chloride to produce 0.6 g of the title compound; m.p.=65°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897490
Source datasetuspto-grants-1990_01
ORD IDord-1280e92bad6543588ed1cc958e90a50a
Source noteuspto-grants-1990_01