HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 514670Erstellt: 25. Oktober 2026
Methacryloyl chloride → (E)-N-methacryloylbut-2-enamide
https://huagongshe.com/reaction/514670
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methacryloyl chloride | HCID 13528 | — |
| Edukt | 2-Butenamide | HCID 5354487 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (E)-N-methacryloylbut-2-enamide | HCID 72205393 | — |
Reaktionsschritte
Experimental Procedure: To a suspension of (E)-but-2-enamide (1.0 equiv) in 3.5 mL THF was added n-BuLi in hexanes (2.5 M,1.2 equiv) slowly at −78° C. The reaction mixture was warmed up to room temperature and stirred for 8 h before a solution of methacryloyl chloride (2.0 equiv) in 2 mL of THF was added drop wise at −78° C. The reaction mixture was allowed to warm up to rt overnight. The crude reaction mixture was diluted with ethyl acetate, and quenched with cold NH4Cl(aq, sat), and the organic layer separated. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine and dried over MgSO4. After filtration and evaporation under reduced pressure, the residue was purified by column chromatography to yield the pure compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09108923B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-b6e713ba9a044e2b97d5ba2a0a95dbc8 |
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| Quellennotiz | uspto-grants-2015_08 |
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