HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Diiodobutane → 2-(4-(Pyrimidin-2-ylthio)butylthio)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Diiodobutane | HCID 12337 | — |
| Reactant | HCID 178418793 | HCID 178418793 | — |
| Reactant | HCID 178473702 | HCID 178473702 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-(Pyrimidin-2-ylthio)butylthio)pyrimidine | HCID 57804723 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576165B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-323fed9735a84769a9e34cba80197fb7 |
| Source note | uspto-grants-2009_08 |