HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → 2,6-DI-Tert-butyl-4-hydroxyphenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Acetoxy-3,5-di-tert-butylanisole | HCID 11821954 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-DI-Tert-butyl-4-hydroxyphenyl acetate | HCID 11139998 | 80% |
Reaction Steps
4-Acetoxy-3,5-di-tert-butylanisole (0.50 g) was dissolved in dichloromethane (2 ml). After cooling with ice, trimethylsilyl iodide (0.31 ml) was added dropwise. The mixture was allowed to warm slowly to room temperature and stirred for 2 days; thereafter, a saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture. The mixture was subjected to extraction with diethyl ether and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel chromatography (15% ethyl acetate in n-hexane) to afford 4-acetoxy-3,5-di-tert-butylphenol [0.38 g (yield, 80%)] as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574178 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-76f62dfe60f74e48881eae31ffc232e2 |
| Source note | uspto-grants-1996_11 |