HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338073Generated: October 29, 2026
Potassium Carbonate → 2-(Diallylamino)-1-(5-fluoro-2-thienyl)ethanone
https://huagongshe.com/reaction/338073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diallylamine | HCID 31279 | — |
| Reactant | 2-Bromo-1-(5-fluorothiophen-2-yl)ethanone | HCID 59706947 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Diallylamino)-1-(5-fluoro-2-thienyl)ethanone | HCID 86697889 | 87.4% |
Reaction Steps
To a stirred solution of 2-bromo-1-(5-fluorothiophen-2-yl)ethanone (13.28 g, 59.53 mmol) in acetonitrile (298 mL) at 0° C. under nitrogen is added potassium carbonate (10.70 g, 77.39 mmol) and diallylamine (9.54 mL, 77.39 mmol). The mixture is allowed to slowly warm to room temperature with stiffing over 16 hours then diluted with ethyl acetate (500 mL) and water (200 mL). The phases are separated and the aqueous phase extracted twice with ethyl acetate (100 mL). The combined organic extracts are dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue is purified by silica gel chromatography eluting with hexanes/ethyl acetate (9:1) to give the title compound (12.45 g, 87%) as a yellow oil. ES/MS (m/e): 240 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889856B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-315854cd01334ddf9f975bd69723b5b4 |
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| Source note | uspto-grants-2014_11 |
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