HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504985Generated: November 2, 2026
2-(Ethylamino)ethanol → HCID 68470062, compound
https://huagongshe.com/reaction/504985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Ethylamino)ethanol | HCID 8072 | — |
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68470062 | HCID 68470062 | — |
Reaction Steps
2-Bromothiophene (16.3 g, 0.1 mol), 2-(ethylamino)ethanol (100 ml), Cu metal (0.32 g), CuI (0.85 g), K3PO4(42.4 g) were added to a flask fitted with a magnetic stir bar, a condenser and sealed with a septum. The reaction mixture was stirred at 80° C. for 72 hour under nitrogen position pressure. After the reaction cooled to room temperature, 600 ml water was added and mixture was extracted with ethyl ether (3*200 ml). The combined organic layers were then washed with brine and dried over MgSO4. The solvent was removed in vacuo and the residue was purified by flash chromatography on silica gel eluted with hexane/EtoAc (1:1). The product was obtained as a liquid. Examples of Amination of 2-bromothiophene are shown in Table 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781187B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-88a78813709d44459b35f15ed7c54712 |
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| Source note | uspto-grants-2010_08 |
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