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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625855Generated: October 31, 2026

t-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate → HCID 178436306, compound

https://huagongshe.com/reaction/1625855

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrateHCID 66608203—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178436306HCID 178436306—

Reaction Steps

A solution of the above t-butyl 2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate in trifluoroacetic acid (60 ml) was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate, and the mixture was washed successively with a saturated aqueous sodium hydrogen carbonate solution and brine. The mixture was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give 1-(4-ethylphenyl)-4-hydroxy-3-penten-2-one (4.00 g) as yellow oil. APCI-Mass m/Z 205 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-aaff97ec30a2469280c559d3cfe4425b
Source noteuspto-grants-2014_07