HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 909396Erstellt: 25. Oktober 2026
Hydrogen Peroxide → 2-Ethyl-1-hydroxy-3-hexanone
https://huagongshe.com/reaction/909396
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | 2-Ethyl-1,3-Hexanediol | HCID 7211 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | Phosphoric acid, disodium salt, dodecahydrate | HCID 61456 | — |
| Katalysator | Sodium Tungstate Dihydrate | HCID 150191 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 2-Ethyl-1-hydroxy-3-hexanone | HCID 11116179 | — |
Reaktionsschritte
Into 5.90 g of 35% hydrogen peroxide solution (60.0 mmol), 720 mg of disodium phosphate dodecahydrate (2.0 mmol) and 165 mg of sodium tungstate dihydrate (0.5 mmol) were dissolved to prepare a mixed reagent (pH 6.5). After 7.3 g of 2-ethyl-1,3-hexanediol (50.0 mmol) was dissolved into 100 mL of N,N-dimethylacetamide, the resultant was heated to 90° C., and the above mixed reagent was added. After the reaction was continued at 90° C. for four hours, 100 mL of toluene and 100 g of 10% brine were added for liquid separation. The aqueous layer was extracted three times with 100 mL of toluene, and all the organic layers were combined and concentrated under reduced pressure. The concentrated liquid was separated and purified by silica gel chromatography (developing solvent hexane:ethyl acetate=3:2) to obtain oily 2-ethyl-1-hydroxy-3-hexanone. The yield was 5.33 g (73%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08017793B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-85edff2eb09a47ca976ed5f7cb9545a4 |
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| Quellennotiz | uspto-grants-2011_09 |
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