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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103945Generated: October 31, 2026

1,4-Diiodobutane → 2-(4-(Pyrimidin-2-ylthio)butylthio)pyrimidine

https://huagongshe.com/reaction/2103945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DiiodobutaneHCID 12337—
ReactantHCID 178418793HCID 178418793—
ReactantHCID 178473702HCID 178473702—
SolventEthanolHCID 702—
Product2-(4-(Pyrimidin-2-ylthio)butylthio)pyrimidineHCID 5780472386%

Reaction Steps

20 mmole of 2-mercaptopyrimidine was dissolved in 20 ml of ethanol with stirring. 20 mole of EtOK (24 weight % in ethanol) was added to the solution, stirred for 5 minutes. Then, about 10 mmole of 1,4-diiodobutane was added, and stirred overnight. The white precipitate was removed by filtration, the solvent in the filtrate was removed in vacuum. The obtained solid was dissolved in CH2Cl2, and separated with a Si gel column (solvents: 1 ethylacetate/1 hexane in volume). Yield: 86%. 1H NMR (CDCl3) of PyrC4: δ(ppm) 8.50 (4H, d, JH-H=4.77), 6.94 (2H, t, JH-H=4.77), 3.20 (4H, t, JH-H=6.93), and 1.91 (4H, t, JH-H=6.93).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576165B2
Source datasetuspto-grants-2009_08
ORD IDord-323fed9735a84769a9e34cba80197fb7
Source noteuspto-grants-2009_08