HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856023Generated: October 30, 2026
Water → 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol
https://huagongshe.com/reaction/856023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2-Bromoethoxy)tetrahydro-2H-pyran | HCID 86621 | — |
| Reactant | n-Methyl-4-(trifluoromethoxy)aniline | HCID 737351 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol | HCID 69479763 | 54.4% |
Reaction Steps
A mixture of N-methyl-(4-trifluoromethoxyphenyl)amine (4.83 g, 24.24 mmol), 2-(2-bromoethoxy)-tetrahydropyran (6.1 g, 29.03 mmol), and potassium carbonate (3.84 g, 27.76 mmol) in DMF (20 ml) was stirred at 100° C. for 5 hours. The reaction mixture was allowed to return to room temperature, poured into water, and extracted with ethyl acetate twice. The extract was washed with water twice and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate=20/1) to afford 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol (3.1 g, yield 53%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-073843149b46452298e48ccbed9587f2 |
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| Source note | uspto-grants-2007_08 |
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