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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705851Generated: November 2, 2026

Ethyl butyrate → 5-Ethyl-2-thiouracil

https://huagongshe.com/reaction/705851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl butyrateHCID 7762—
ReactantEthyl formateHCID 8025—
ReactantThioureaHCID 2723790—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Ethyl-2-thiouracilHCID 300204282%

Reaction Steps

To a suspension of potassium tert-butoxide (12.08 g, 108 mmol) in THF (40 mL) was added a solution of ethyl butyrate (5.69 mL, 43.0 mmol) and ethyl formate (6.93 mL, 86 mmol) in diethyl ether (40.0 mL) dropwise under nitrogen. The mixture was stirred at room temperature for 3 h. After removing the solvent, the residue oil was dissolved in isopropanol (350 mL), and thiourea (6.55 g, 86 mmol) was added. The mixture was stirred at reflux overnight, and then concentrated in vacuo to get a solid. The solid was dissolved in water, adjusted pH to 4 with AcOH, and extracted by DCM. The organic layer was dried over Na2SO4, filtered and concentrated to afford the title compound (5.5 g, 82% yield) as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-267e12404e0a49179f013a737b5f339a
Source noteuspto-grants-2015_11