HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Ethyl 4-[6-acetyl-3-[2-(4-acetyl-3-hydroxy-2-propylphenylthio)-ethoxy]-2-propylphenoxy]butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Hydroxy-3-propyl-4-sulfanylphenyl)ethan-1-one | HCID 13295518 | — |
| Reactant | Ethyl 4-[6-acetyl-3-(2-chloroethoxy)-2-propylphenoxy]butyrate | HCID 15712390 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 4-[6-acetyl-3-[2-(4-acetyl-3-hydroxy-2-propylphenylthio)-ethoxy]-2-propylphenoxy]butyrate | HCID 15712393 | 82.8% |
Reaction Steps
A mixture of ethyl 4-[6-acetyl-3-(2-chloroethoxy)-2-propylphenoxy]butyrate (0.60 g), (2-hydroxy-4-mercapto-3-propylphenyl)ethanone (0.51 g), potassium iodide (0.1 g) and potassium carbonate (0.65 g) in acetone (40 ml) was heated and refluxed with stirring for 19 hours. After cooled, inorganic materials were separated by filtration and the filtrate was concentrated. The resultant residue was separated and purified through silica gel column chromatography (eluting with benzene:ethyl acetate=15:1, then 9:1) to give the title compound (0.73 g, 82.8%) as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE038921E1 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-2391c019b6244bd3b15092931190dbb3 |
| Source note | uspto-grants-2005_12 |