HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717133Generated: October 25, 2026
p-Bromoacetophenone → 2-(4-Bromophenyl)propan-2-ol
https://huagongshe.com/reaction/717133
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Bromophenyl)propan-2-ol | HCID 12681920 | 99.4% |
Reaction Steps
1-(4-Bromophenyl)ethanone (9.25 g, 46.5 mmol) was dissolved in tetrahydrofuran (200 mL). The solution was cooled in a −50° C. bath. Methylmagnesium bromide (3M in ether, 46.5 mL, 139 mmol) was added over a 15 min period. The reaction was allowed to warm to room temperature and then stirred for 20 h. The reaction was quenched with saturated ammonium chloride and then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered and concentrated to give an oil. The oil was purified on a silica gel column (0-20% ethyl acetate in hexanes) to give the product a colorless oil (9.1 g, 46.2 mmol, 91% yield). MS (ESI) m/z 197.1 [M]+, 199.1 [M+2]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193692B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-86522330519141088ca8b4867b553901 |
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| Source note | uspto-grants-2015_11 |
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