HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene carbonate → 2-[4'-Fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-yloxy]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | 2-(p-Fluorophenyl)-6-isopropylphenol | HCID 14663966 | — |
| Catalyst | Tetraethylammonium Iodide | HCID 6225 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4'-Fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-yloxy]ethanol | HCID 19004417 | 26% |
Reaction Conditions
| Temperature | 155 °C |
|---|
Reaction Steps
A mixture of 4'-fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-ol (1.84 g), ethylene carbonate (0.78 g) and tetraethylammonium iodide (0.68 g) was heated in an oil bath at 155° C. for 2 hours, then was cooled and taken up in dichloromethane. The solution was washed in turn with water, 1N sodium hydroxide, 1N hydrochloric acid and brine, then was dried (MgSO4) and evaporated. The residual material was chromatographed over 70 g of silica gel (ethyl acetate-hexane; 3:7) to provide 0.57 g of 2-[4'-fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-yloxy]ethanol. The compound was crystallized from hexane to give the analytical sample, mp 77°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344843 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-8063b8bd046e43a5a5f68fc3ef2b7a3a |
| Source note | uspto-grants-1994_09 |