HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1951395Erstellt: 26. Oktober 2026
Acetic Acid → 4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methylbenzonitrile
https://huagongshe.com/reaction/1951395
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Acetylacetone | HCID 31261 | — |
| Edukt | 4-Formyl-3-methylbenzonitrile | HCID 10909695 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methylbenzonitrile | HCID 59603030 | — |
Reaktionsschritte
950 mg (6.54 mmol) of 3-methyl-4-formylbenzonitrile [S. Levesque et al., Bioorg. Med. Chem. Lett. 11, 3161-3164 (2000], 655.2 mg (6.544 mmol) of 2,4-pentanedione, 589.5 mg (9.82 mmol) of acetic acid and 111.5 mg (1.31 mmol) of piperidine are dissolved in 35 ml of dichloromethane and heated under reflux with an inverse water trap overnight. Cooling is followed by washing twice with water, and the organic phase is dried with magnesium sulfate. The solvent is removed in a rotary evaporator and the residue is purified by column chromatography (silica gel, mobile phase: initially dichloromethane, then isohexane/ethyl acetate 3:1). After concentration of the product fractions, the residue is crystallized from diethyl ether and dried under high vacuum. 1.12 g (75.3% of theory) of the title compound are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08404709B2 |
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| Quelldatensatz | uspto-grants-2013_03 |
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| ORD ID | ord-ffc25bb006974dd58b30decbfe449b09 |
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| Quellennotiz | uspto-grants-2013_03 |
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