HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418147Generated: October 28, 2026
Diethyl Ether → 1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanone
https://huagongshe.com/reaction/418147
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 66650354 | HCID 66650354 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Product | 1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanone | HCID 66650336 | 34% |
Reaction Steps
To a solution of 3-ethoxy-4-trifluoromethyl-benzonitrile from step 5 (5.00 g, 23.2 mmol), copper(I) bromide (100 mg, 0.7 mmol), tert.-butyldimethylchlorosilane (4.20 g, 27.9 mmol) in dry THF (30 mL) at −70° C. was drop wise added a 3 M methylmagnesium bromide solution in diethyl ether (13.2 mL, 39.6 mmol). The mixture was stirred at −70° C. for 10 min, then was warmed up to 0° C. and stirring was continued at 0° C. for further 2 h under nitrogen atmosphere. Poured the reaction mixture onto ice and sat. NH4Cl-sol., extracted three times with diethyl ether, washed the combined organic layers with brine, dried over MgSO4. Removal of the solvent in vacuum left a brown oil, which was purified by silica gel column chromatography with heptane/EtOAc 4:1 to give the title compound as a yellow liquid (1.84 g, 34%). MS (EI) 232 [M].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093263B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-8edfbd7ffe9544b4b36944cfa7743048 |
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| Source note | uspto-grants-2012_01 |
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