HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625854Generated: November 2, 2026
Citric Acid → t-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate
https://huagongshe.com/reaction/1625854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | 4-Ethylphenylacetyl chloride | HCID 15578354 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | t-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate | HCID 66608203 | — |
Reaction Steps
A suspension of magnesium chloride (1.74 g) in dichloromethane (30 ml) was cooled to 0° C., and thereto were added t-butyl acetoacetate (3.03 ml) and pyridine (2.96 ml), and successively was added a solution of the above 4-ethylphenylacetyl chloride in dichloromethane (30 ml). The mixture was stirred at the same temperature for 2.5 hours, and an aqueous citric acid solution was added thereto. The mixture was extracted with chloroform. The extract was washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to give t-butyl 2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate (4.75 g) as pale yellow oil. APCI-Mass m/Z 322 (M+NH4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785403B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-4915531292404465b1541f97a6d917a9 |
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| Source note | uspto-grants-2014_07 |
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