HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387641Generated: October 30, 2026
Potassium Carbonate → 2-(2-bromophenyl)-N-(2-ethoxyethyl)ethanamine
https://huagongshe.com/reaction/387641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethoxyethylamine | HCID 66970 | — |
| Reactant | HCID 15364878 | HCID 15364878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-bromophenyl)-N-(2-ethoxyethyl)ethanamine | HCID 68470512 | — |
Reaction Steps
3.5 g of 2-(2-bromophenyl)ethyl methanesulfonate, 5.59 g of 2-ethoxyethanamine, 8.67 g of potassium carbonate and 70 cm3 of tetrahydrofuran are stirred under the reflux of the solvent under an inert atmosphere for 48 h. The heating is stopped, then the reaction mixture is filtered. The insoluble material is washed twice with ethyl acetate. The filtrate is concentrated using a rotary evaporator under reduced pressure (5 kPa). The product obtained is purified by flash chromatography over silica (column: 330 g; particle size: 20-40 μm, spherical; eluent: 100% ethyl acetate to 90% ethyl acetate/10% methanol gradient). After concentrating the fractions under reduced pressure, 2.45 g of 2-(2-bromophenyl)-N-(2-ethoxyethyl)ethanamine are obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372864B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ec8a03b675bb4e06be24ae3e8cea9adb |
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| Source note | uspto-grants-2013_02 |
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