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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromophenyl)propan-2-olHCID 1268192099.4%

Reaction Conditions

Temperature-50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193692B2
Source datasetuspto-grants-2015_11
ORD IDord-86522330519141088ca8b4867b553901
Source noteuspto-grants-2015_11