HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974487Generated: October 29, 2026
Tert-butyl acetoacetate → HCID 54272216, compound
https://huagongshe.com/reaction/974487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 53912652 | HCID 53912652 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54272216 | HCID 54272216 | — |
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 chromatrography on silica gel eluting with methanol in methylene choride to produce 0.6 g of the title compound; m.p.=65°-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068346 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-05ddef92e90e417d9095f974dc1f826f |
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| Source note | uspto-grants-1991_11 |
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