HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Phenol, 2,6-bis(1,1-dimethylethyl)-4-[[(dimethylphenylsilyl)methyl]thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Di-tert-butyl-4-mercaptophenol | HCID 70370 | — |
| Reactant | (Chloromethyl)dimethylphenylsilane | HCID 74598 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Phenol, 2,6-bis(1,1-dimethylethyl)-4-[[(dimethylphenylsilyl)methyl]thio]- | HCID 11485998 | — |
Reaction Steps
Mix 2,6-di-t-butyl-4-mercaptophenol (2.4 g, 10mmol), potassium carbonate (1.4 g, 10 mmol), chloromethyldimethylphenylsilane (1.9 g, 10 mmol) and dimethylformamide (50 mL) and stir overnight at room temperature under argon atmosphere. Dilute the mixture with ice-water and extract with ethyl ether. Wash the ethereal layer with water, then brine, filter through flourosil-Na2SO4, and evaporate to an orange oil (3.5 g). Purify the product by first distilling (bp 160°-170° C. @0.1 mm Hg), then subjecting to silica gel chromatography (CCl4 :CHCl3 /1:1) to obtain the title compound as a light yellow oil which slowly crystallizes to a whim waxy solid (2.3 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05677291 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-b31d51ada0214b6e9a7b49cbf07c64a8 |
| Source note | uspto-grants-1997_10 |