HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904977Generated: November 3, 2026
Sodium hydride → 2-(3-Chloro-4-ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-fluorophenoxy)benzyl ether
https://huagongshe.com/reaction/1904977
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Fluorophenoxy)benzyl Bromide | HCID 2737456 | — |
| Reactant | 2-(3-Chloro-4-ethoxyphenyl)-3,3,3-trifluoropropanol | HCID 20036685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Chloro-4-ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-fluorophenoxy)benzyl ether | HCID 14580815 | 35.6% |
Reaction Steps
Under a nitrogen atmosphere, 60 mg of sodium hydride (60% oil dispersion) was added to 10 ml of dry THF. A solution of 0.41 g of 2-(3-chloro-4-ethoxyphenyl)-3,3,3-trifluoropropanol and 1.43 g of 3-(4-fluorophenoxy)benzyl bromide in 10 ml of dry THF 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 (40:1) mixture] to obtain 255 mg of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04840971 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-15c3f46d6ff44ef7b55f69dc6106e831 |
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| Source note | uspto-grants-1989_06 |
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