HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1435164Erstellt: 26. Oktober 2026
Ethyl 2-methylacetoacetate → 5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid
https://huagongshe.com/reaction/1435164
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Edukt | 1,4-Butane sultone | HCID 15411 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid | HCID 58084006 | 122,6% |
Reaktionsschritte
Ethyl 2-methylacetoacetate (43.2 g) in N,N-dimethylformamide (25 ml) was added to a suspension of sodium hydride (12.0 g of 60% NaH in mineral oil) in N,N-dimethylformamide (100 ml), dropwise with ice-bath cooling. This mixture was allowed to warm to ambient temperature for 30 mins before re-cooling. 1,4-butanesultone (40.8 g) in N,N-dimethylformamide (25 ml) was then added dropwise. The final mixture was heated at 50° C. for 18 hrs, then quenched with 50 ml of water. The solvent was evaporated under vacuum; the residue was partitioned between water and diethyl ether. The aqueous layer was collected, washed with fresh diethyl ether and evaporated under vacuum; final drying was under high vacuum over phosphorus pentoxide. A yield of 103 g of 5-(ethoxycarbonyl)-5-methyl-6-oxoheptane-1-sulfonic acid was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07615646B2 |
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| Quelldatensatz | uspto-grants-2009_11 |
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| ORD ID | ord-7663d7c9aae042e28aae309888a66498 |
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| Quellennotiz | uspto-grants-2009_11 |
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