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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251023Generated: November 3, 2026

Ethanol → HCID 18325846, compound

https://huagongshe.com/reaction/1251023

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 numberUS06340772B1
Source datasetuspto-grants-2002_01
ORD IDord-a6a77fae6c4140e8b0ba6bd4036633cc
Source noteuspto-grants-2002_01