HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30831Generated: October 26, 2026
Bromobenzene → 4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric Acid
https://huagongshe.com/reaction/30831
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 2,2-Dimethylsuccinic anhydride | HCID 87067 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric Acid | HCID 21985757 | 63% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423156B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-c7b93df0ff2d4a47978180e5bed6eed4 |
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| Source note | uspto-grants-2008_09 |
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