HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 907656Erstellt: 23. Oktober 2026
Bromobenzene → 4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric Acid
https://huagongshe.com/de/reaction/907656
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bromobenzene | HCID 7961 | — |
| Edukt | 2,2-Dimethylsuccinic anhydride | HCID 87067 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | 1,1-Dichloroethane | HCID 6365 | — |
| Produkt | 4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric Acid | HCID 21985757 | 63% |
Reaktionsschritte
To a chilled solution (ice/water bath) of bromobenzene (7.71 g, 49.1 mmol) and 3,3-dimethyldihydro-2,5-furandione (5.99 g, 46.7 mmol) in dichloroethane (150 mL) was added aluminum trichloride (13.28 g, 99.58 mmol). The ice bath was removed and the reaction mixture was stirred at rt overnight. The mixture was again chilled in an ice/water bath, and then quenched with 1 M aqueous hydrochloric acid. Water (70 mL) was added and the layers were separated. The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (Biotage apparatus, 17:83 ethyl acetate/hexane) to give 4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid as a white solid (8.34 g, 63%). LC-MS: ret. time 2.79 min; m/z 284.8 (MH+); 1H NMR (300 MHz, CDCl3) δ 1.36 (s, 6H), 3.27 (s, 2H), 7.60 (d, 2H), 7.81 (d, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08013166B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-75447bba3b514e409f443015d7bfb054 |
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| Quellennotiz | uspto-grants-2011_09 |
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