HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329801Erstellt: 25. Oktober 2026
Acetic Acid → Methyl 4-(acetyloxy)-3-oxobutanoate
https://huagongshe.com/reaction/329801
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Methyl 4-chloroacetoacetate | HCID 36240 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Methyl 4-(acetyloxy)-3-oxobutanoate | HCID 13130412 | 61% |
Reaktionsschritte
108 g (1.1 mol) of potassium acetate and 11.4 g (0.05 mol) of benzyltriethylammonium chloride are suspended in 900 ml of acetonitrile, treated with 50 ml of acetic acid and heated to reflux temperature. Within 31/2 hours there are added dropwise thereto 150.5 g (1 mol) of methyl 4-chloroacetoacetate in 100 ml of acetonitrile and the mixture is subsequently held at reflux temperature for 4 hours. The reaction mixture is washed 3 times with 200 ml of 5% NaH2PO4 solution each time and the aqueous phases are back-extracted with 200 ml of CH2Cl2. The combined organic phases are dried over magnesium sulphate and concentrated on a rotary evaporator. The crude product distils at 76°-85° C./0.6 mbar and gives 106.17 g (61%) of methyl 4-acetoxyacetoacetate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04892966 |
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| Quelldatensatz | uspto-grants-1990_01 |
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| ORD ID | ord-8c3bf2c931e84e6699fd0c91310bafde |
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| Quellennotiz | uspto-grants-1990_01 |
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