HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225946Erstellt: 26. Oktober 2026
2,6-Dichlorobenzoic acid → 2,6-Dichlorobenzoyloxymethyl ketone
https://huagongshe.com/reaction/225946
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,6-Dichlorobenzoic acid | HCID 5758 | — |
| Edukt | 1,3-Dibromo-2-propanone | HCID 69952 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2,6-Dichlorobenzoyloxymethyl ketone | HCID 18517524 | — |
Reaktionsschritte
Thus obtained bromomethyl ketone derivative (X, 4.36 g) and 2,6-dichlorobenzoic acid (2.28 g, 1.1 Eq) were dissolved in dimethylformamide (18 ml), KF (1.58 g, 2.5 Eq) was added, and the mixture was stirred for two hours to give 2,6-dichlorobenzoyloxymethyl ketone derivative (XIa). This compound was dissolved in methanol (20 ml) and reacted by adding NaBH4 (412 mg)-methanol solution (40 ml)(−10□˜room temperature, two hours). The reaction was stopped by acetic acid, and the reaction solution was distilled under reduced pressure to remove methanol. The residue was extracted with ethyl acetate (50 ml×2), washed with water and aqueous sodium chloride solution, dried (anhydrous Na2SO4), concentrated under reduced pressure, and separated-purified by column chromatography (ethyl acetate-hexane, 1:5) to give the title compound (4.80 g, Yield 86%) in a diastereomeric form.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07557133B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-f12c119bc359443caf7f777dfcfb8f5d |
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| Quellennotiz | uspto-grants-2009_07 |
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