HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26227Erstellt: 25. Oktober 2026
Sulfuric Acid → Ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate
https://huagongshe.com/reaction/26227
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Ethyl Acetoacetate | HCID 8868 | — |
| Edukt | o-Tolyl-acetyl chloride | HCID 2760632 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | Ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate | HCID 21325237 | — |
Reaktionsschritte
This material was prepared according to the procedure of M. Viscontini and N. Merckling, Helvetica Chimica Acta, 35, 2280 (1952). To 2.65 parts of magnesium turnings was added 15 parts absolute ethanol at room temperature and 0.5 parts of carbon tetrachloride. As soon as the initial reaction subsides 100 parts of dry ether was added. The mixture was stirred without cooling until the reaction ceased, then 19.6 parts of ethyl 3-oxobutanoate in 20 parts of dry ether was added with ice cooling and good stirring. After the resulting precipitate dissolved, the solution was cooled in an ice-salt bath and 16 parts of 2-methylphenylacetyl chloride was slowly added. The mixture was allowed to stand overnight at room temperature and then combined with ice and sulfuric acid. The ether layer was separated, washed with water, dried over sodium sulfate and stripped to give ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate as a crude oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04148918 |
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| Quelldatensatz | uspto-grants-1979_04 |
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| ORD ID | ord-7baf14ecd86f45f5a549cee5a5e5b9b4 |
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| Quellennotiz | uspto-grants-1979_04 |
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