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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401177Generated: November 2, 2026

p-Bromoacetophenone → 2-(4-Bromophenyl)propan-2-ol

https://huagongshe.com/reaction/1401177

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 numberUS08907087B2
Source datasetuspto-grants-2014_12
ORD IDord-de8f676e33fb43c1bc9bd3cc2656ca59
Source noteuspto-grants-2014_12