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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056521Generated: October 30, 2026

Ethyl 3,3-diethoxypropionate → 1-(2-Methoxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

https://huagongshe.com/reaction/1056521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3,3-diethoxypropionateHCID 66389—
Reactant(2-Methoxyethyl)thioureaHCID 1810725—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product1-(2-Methoxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-oneHCID 6240273245%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirring solution of 1-(2-methoxyethyl)thiourea (21.38 g, 159.3 mmol) and ethyl 3,3-diethoxypropanoate (46.5 mL, 239.0 mmol) in MeOH (300 mL) was added a freshly prepared solution of 0.96N sodium methoxide in MeOH (250 mL, 239.0 mmol) dropwise over 30 minutes at room temperature under argon. The reaction mixture was heated to 60° C. for 45 minutes and cooled to room temperature. Solvent was removed under reduced pressure and toluene (250 mL) was added to the residue. The mixture was stirred at reflux for an additional 3 hours and then cooled to room temperature. Water (200 mL) was added and the layers were separated. The aqueous layer was washed with CH2Cl2 (50 mL), neutralized with 2N aqueous HCl and extracted with CH2Cl2 (3×200 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was recrystallized from i-PrOH (200 mL) to give the title compound (13.3 g, 45%) as a light yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399626B2
Source datasetuspto-grants-2016_07
ORD IDord-1a226c9fff72401a9201d2e1eb908263
Source noteuspto-grants-2016_07