HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Di-tert-butyl-4-methylphenol → HCID 19710197, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Ethynyltributyltin | HCID 621176 | — |
| Reactant | HCID 19710221 | HCID 19710221 | — |
| Reactant | HCID 22468310 | HCID 22468310 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19710197 | HCID 19710197 | — |
Reaction Steps
To a solution of 5-trifluoromethanesulfonyloxy-2-(di-n-propylamino)indan (Example 2) in 1,4-dixoane is treated with tri-n-butylethynylstannane, lithium chloride, tetrakis(triphenylphosphlne)palladium(0), and a few crystals of 2,6-di-tert-butyl-4-methylphenol under nitrogen (J. Am. Chem. Soc. 1987, 109, 5478). The mixture is refluxed for 6 h, cooled to room temperature, and treated with pyridine and pyridine fluoride and iluted with diethyl ether. The resulting crude product is purified by chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05708018 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-8a0ee0b2273545a9bad4e13a2ffb1522 |
| Source note | uspto-grants-1998_01 |