HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576059Generated: November 1, 2026
Water → 2-Bromo-1-(4-tert-butylphenyl)ethan-1-one
https://huagongshe.com/reaction/576059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-tert-Butylacetophenone | HCID 13669 | — |
| Reactant | Pyrrolidone trihydrobromide | HCID 20283272 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(4-tert-butylphenyl)ethan-1-one | HCID 2324770 | — |
Reaction Steps
Pyrrolidone trihydrobromide (3.27 g, 10.0 mmol) was added to a solution of 1-(4-tert-butylphenyl)ethanone obtained (1.61 g, 9.13 mmol) in tetrahydrofuran (30 mL) and the mixture was heated to an external temperature of 60° C. and stirred for 30 min. After cooling, water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate and then the desiccant was filtered off, followed by concentration under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane only→hexane:ethyl acetate=9:1) to afford the title compound as a colorless oil (472 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035059B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-f1f4f4e3c8d547a386e2a72372f8552e |
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| Source note | uspto-grants-2015_05 |
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