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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821032Generated: October 31, 2026

Ethyl 3-(3-methoxy-2-methylphenyl)-3-oxopropanoate → Ethyl 3-(3-methoxy-2-methylphenyl)propanoate

https://huagongshe.com/reaction/1821032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3-methoxy-2-methylphenyl)-3-oxopropanoateHCID 68850344—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 3-(3-methoxy-2-methylphenyl)propanoateHCID 6885041283.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution ethyl 3-(3-methoxy-2-methylphenyl)-3-oxopropanoate (137.2 g, 595 mmol, from Step A) in ethyl alcohol (924 mL), 10% Pd—C (13.7 g) was added and 3 atm of hydrogen were applied. The mixture was heated to 60° C. for 20 hr, cooled to ambient temperature and filtered through Celite®. The filtrate was concentrated in vacuo and the residue purified by flash chromatography (2% EtOAc/hexanes) on SiO2 to afford 110.8 g of the title compound as a pale yellow liquid: 1H NMR (500 MHZ, CDCl3) δ 1.25 (t, 3H, J=7.1 Hz), 2.19 (s, 3H), 2.55 (t, 2H, J=8.0 Hz), 2.95 (t, 2H, J=8.0 Hz), 3.82 (s, 3H), 4.14 (q, 2H, J=7.1 Hz), 6.73 (d, 1H, J=8.2 Hz), 6.78 (d, 1H, J=7.6 Hz), 7.10 (d, 1H, J=7.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605171B2
Source datasetuspto-grants-2009_10
ORD IDord-bbedefefb6dc4ccea9266473bf9f9071
Source noteuspto-grants-2009_10