HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 131711331, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22761172 | HCID 22761172 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 131711331 | HCID 131711331 | 97.6% |
Reaction Steps
As described in Example 30, a mixture of 3.13 g of p-tert.-butylphenol, 0.755 g of 60% sodium hydride-oil dispersion, 3.5 g of potassium iodide, one ml of hexamethylphosphoramide and 7.9 g of methyl bromo{p-[3-(p-chlorophenoxy)propoxy]phenyl}acetate in 70 ml of tetrahydrofuran is refluxed for 18 hours and worked-up to give 9.0 g of an oil. The oil is chromatographed over silica gel with dichloromethane as eluent to give 7.4 g of oil which is crystallized from petroleum ether-ether to give 5.7 g of white crystals, mp 98°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125732 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-03499f8ad2884687a68074c121ab8ac7 |
| Source note | uspto-grants-1978_11 |