HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5565Erstellt: 24. Oktober 2026
Hydrochloric Acid → 2-Butyryl-5-cyclohexylcyclohexane-1,3-dione
https://huagongshe.com/de/reaction/5565
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dimethyl malonate | HCID 7943 | — |
| Edukt | Butyryl chloride | HCID 8855 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-Cyclohexylbut-1-en-3-one | HCID 95597 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-Butyryl-5-cyclohexylcyclohexane-1,3-dione | HCID 19796579 | 84,1% |
Reaktionsschritte
132 g of dimethyl malonate, 180 g of 30% strength sodium methylate, 152 g of 1-cyclohexylbut-1-en-3-one and 106.5 g of butyryl chloride are reacted in 1 liter of toluene, in a manner similar to that described in Example 1. 5 g of 4-N,N-dimethylaminopyridine are added to the reaction mixture thus obtained and the batch is stirred for 4 hours at 100° C. and then cooled to room temperature. It is then extracted twice with a total of 3.5 moles of sodium hydroxide in 1.5 liters of water and the combined alkaline extracts are stirred for 2 hours at 80° C. They are then acidified with about 270 ml of concentrated hydrochloric acid at 50° C., the oil obtained is extracted with methylene chloride and the extracts are washed with water and evaporated in vacuo. 222 g (84%) of 2-butyryl-5-cyclohexylcyclohexane-1,3-dione are obtained as a pale brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05245041 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-c5320739ecb94875895071e346290d87 |
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| Quellennotiz | uspto-grants-1993_09 |
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