HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904973Generated: October 27, 2026
Sodium hydride → 2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-fluorophenoxy)benzyl ether
https://huagongshe.com/reaction/1904973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Fluorophenoxy)benzyl Bromide | HCID 2737456 | — |
| Reactant | (RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)propan-3-ol | HCID 10681171 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-fluorophenoxy)benzyl ether | HCID 14580814 | 77.9% |
Reaction Steps
Under a nitrogen atmosphere, 171 mg of sodium hydride (60% oil dispersion) was added to 15 ml of dry DMF. A solution of 1.0 g of 2-(4-ethoxyphenyl)-3,3,3-trifluoropropanol and 1.08 g of 3-(4-fluorophenoxy)-benzyl bromide in 20 ml of dry DMF was then added with ice-cooling, and the reaction solution was stirred with ice-cooling for 1 hour and at room temperature for 12 hours. Thereafter, the reaction mixture was poured into dilute HCl-ice water and extracted twice with diethyl ether. The ether layers were combined, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure, and the residue was subjected to column chromatography on silica gel [eluted with n-hexane/ethyl acetate (25:1) mixture] to obtain 1.30 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04840971 |
|---|
| Source dataset | uspto-grants-1989_06 |
|---|
| ORD ID | ord-3db15275476d4c50894ba5f8873e0988 |
|---|
| Source note | uspto-grants-1989_06 |
|---|