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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650315Generated: October 30, 2026

Ethanol → HCID 18325846, compound

https://huagongshe.com/reaction/650315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl vinyl ketoneHCID 6570—
Reactantmethyl 3-(4-methylphenyl)-3-oxopropanoateHCID 291780—
CatalystSodium ethoxideHCID 2723922—
ProductHCID 18325846HCID 18325846—

Reaction Steps

To a stirred solution of methyl 3-(4-methylphenyl)-3-oxopropanoate(2.28 g, 11.1 mmol) in EtOH(10 ml), NaOEt(11 mg, 0.16 mmol) was added and methyl vinyl ketone(2.0 g, 27.8 mmol) was added dropwise less than 25° C. After stirring the reaction mixture for 30 min. less than 25° C., the solvent was evaporated under reduced pressure. Dil.HCl aq. was added to the residue and extracted by EtOAc. The organic layer was washed with water and brine, dried over MgSO4. After removal of the solvent, the residue was purified by column chromatography on silica gel with n-hexane-AcOEt to afford 2.73 g of ethyl 2-((4-methylphenyl)carbonyl)-5-oxohexanoate as a pale yellow oil (y=89.0%). 1H-NMR(ppm, 300 MHz, CDCl3) δ 7.92(2H, d, J=8.0 Hz), 7.28(2H, d, J=8.0 Hz), 4.41(1H, t, J=7.0 Hz), 4.14(2H, q, J=6.9 Hz), 2.55-2.60(2H, m), 2.13(3H, s), 1.17(3H, t, J=6.9 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271418B1
Source datasetuspto-grants-2001_08
ORD IDord-2fbc55ac3b9d48a49a8291871b51828a
Source noteuspto-grants-2001_08