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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474609Generated: October 29, 2026

Ethyl butyrate → 5-Ethyl-2-thiouracil

https://huagongshe.com/reaction/474609

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 dissloved 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 numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-9ede782568ba4fff862f24bcc82dab25
Source noteuspto-grants-2014_01