HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 591046Erstellt: 25. Oktober 2026
Diethyl Ether → 1-(2-Hydroxy-6-methylphenyl)ethanone
https://huagongshe.com/reaction/591046
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Ethyl 2-hydroxy-6-methylbenzoate | HCID 584222 | — |
| Edukt | HCID 178418573 | HCID 178418573 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-(2-Hydroxy-6-methylphenyl)ethanone | HCID 11159401 | 72,1% |
Reaktionsschritte
A solution of methyl magnesium bromide 3M in diethyl ether (18.5 mL, 55.5 mmol) and triethylamine (6.0 mL, 44.4 mmol) in anhydrous toluene (14 mL) was cooled to 0° C. 6-methylsalicylic acid ethyl ester (2.0 g, 11.1 mmol) in anhydrous toluene (14 mL) was added dropwise and the reaction mixture was stirred at room temperature for 16 hours. A saturated solution of ammonium chloride (10 mL) was added and the mixture was filtered over Celite®. The filtrate was diluted with ethyl acetate (20 mL) and water (10 mL) and layers were separated. The organic layer was washed with brine (10 mL), dried over sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 9/1) to provide the desired ketone (26a) (1.21 g, 8.0 mmol, 72%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09238026B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-b494766faafc49a280d668843bc62aec |
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| Quellennotiz | uspto-grants-2016_01 |
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