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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032455Generated: November 1, 2026

Ethyl Acetoacetate → HCID 14851338, compound

https://huagongshe.com/reaction/1032455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14851337HCID 14851337—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14851338HCID 1485133887%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a hexane washed suspension of NaH (1.23 g, 30.7 mmol) in THF (20 ml) at 0° C. under an inert atmosphere, was added a solution of ethyl acetoacetate (3.66 ml, 28.7 mmol) in THF (20 ml). The resulting clear solution was stirred at 0° C. for 15 minutes before n-BuLi (13.1 ml, 28.7 mmol) was added dropwise. This orange solution was stirred at 0° C. for 15 minutes before it was cooled to -78° C. and a solution of the unsaturated aldehyde (7.50 g, 19.2 mmol, Step E) in THF (100 ml) was added dropwise. The reaction was stirred at -78° C. for one hour and then it was quenched by adding 4 ml glacial acetic acid and removing the cooling bath. The reaction mixture was partitioned between Et2O and saturated aqueous K2CO3 solution. The organic extracts were dried (MgSO4) and evaporated to give an orange solid. Recrystallization from hexanes gave 8.71 g (87%) of product as a pale yellow orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957971
Source datasetuspto-grants-1990_09
ORD IDord-96c0ff7c72f54bcc9675e6eedd61ace1
Source noteuspto-grants-1990_09