HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenol → HCID 20131576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 20131574 | HCID 20131574 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 20131576 | HCID 20131576 | 49.1% |
Reaction Steps
3.0 g of 2-tert.-butyl-2-[(1H-1,2,4-triazol-1-yl)fluoromethyl]-oxirane, 1.7 g of 4-fluorophenol and 0.3 g of potassium p-fluorophenate in 10 ml of diethylene glycol dimethyl ether are stirred at 140° C. for 5 hours. After cooling, the mixture is taken up in ice water and extracted with ethyl acetate. The combined organic phases are washed with water, saturated sodium chloride solution and 2N sodium hydroxide solution and again with saturated sodium chloride solution, dried over sodium sulfate and evaporated. Crystallisation from a 1:4 ether/hexane mixture gives 2.3 g of 1-(4-fluorophenoxy)-2-tert.-butyl-2-hydroxy-3-fluoro-3-(1H-1,2,4-triazol-1-yl)-propane, melting point 89°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04758670 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-0cf6473708a64ccd8605cb6c182a5003 |
| Source note | uspto-grants-1988_07 |