HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(4-Ethoxyphenoxy)-2-isopropylphenyl benzyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Ethoxyphenol | HCID 12150 | — |
| Reactant | 1-(Benzyloxy)-4-bromo-2-isopropylbenzene | HCID 21466345 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(4-Ethoxyphenoxy)-2-isopropylphenyl benzyl ether | HCID 21466253 | 37.1% |
Reaction Steps
A mixture of 10 g of 4-bromo-2-isopropylphenyl benzyl ether, 4.7 g of 4-ethoxyphenol, 4.7 g of potassium carbonate, 0.30 g of copper powder, 0.30 g of cuprous iodide and 30 ml of pyridine was stirred at 130° C. to 140° C. for 24 hours. The reaction solution was cooled to room temperature, poured into ice-water and then acidified by adding 10% hydrochloric acid. The solution was extracted with 100 ml of diethyl ether, washed in turn with 10% hydrochloric acid, an aqueous 10% sodium hydroxide solution and a saturated saline solution, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 4.4 g of 4-(4-ethoxyphenoxy)-2-isopropylphenyl benzyl ether (yield, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530015 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-e61f5b7aa21e4424b337909c81d83b33 |
| Source note | uspto-grants-1996_06 |