HuagongsheHuagongshe Chemistry Print Report · For research reference only
Probucol → {2,6-Di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-1-methyl-ethylsulfanyl]-phenoxy}-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Probucol | HCID 4912 | — |
| Reactant | Ethyl iodoacetate | HCID 12183 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {2,6-Di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-1-methyl-ethylsulfanyl]-phenoxy}-acetic acid ethyl ester | HCID 11157727 | 27.4% |
Reaction Steps
To a solution of probucol (0.5 g, 0.97 mmol) in dimethylformamide (1.5 mL) were added ethyl iodoacetate (0.31 g, 1.45 mmol) and 40% potassium fluoride on alumina (0.7 g, 4.8 mmol). The mixture was stirred for 24 hours and then diluted with ether (25 mL), filtered and washed with water (2×5 mL). The ether layer was dried over MgSO4, filtered and concentrated. Silica gel chromatography (hexanes/ether 5:95) yielded 160 mg of {2,6-di-tert-butyl-4-[1-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-1-methyl-ethylsulfanyl]-phenoxy}-acetic acid ethyl ester which was used directly for the next step of reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07271274B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-5b15f5d83112436083226b23dd62dec0 |
| Source note | uspto-grants-2007_09 |