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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223054Generated: November 4, 2026

1-(4-Bromophenyl)propan-2-one → 1-(4-Bromophenyl)-2-methylpropan-2-ol

https://huagongshe.com/reaction/2223054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)propan-2-oneHCID 736332—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-(4-Bromophenyl)-2-methylpropan-2-olHCID 31678584%

Reaction Steps

A solution of 4-bromophenylacteone (6.85 g, 32 mmol) in diethyl-ether (100 ml) was cooled to 0° C. and treated with methylmagnesium bromide (23.5 ml of a 3M solution in diethyl-ether, 70 mmol). The reaction mixture was allowed to warm gradually to room temperature. After 2 hours the reaction was quenched by addition of saturated aqueous ammonium chloride (200 ml). The organic phase was separated and washed with saturated sodium chloride (100 ml), dried (sodium sulfate) and reduced in vacuo. Purification by flash column chromatography on silica gel eluting with pentane:dichloromethane (60:40 changing to 0:100, by volume) gave the title compound as a colourless oil (6.23 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375100B2
Source datasetuspto-grants-2008_05
ORD IDord-041b0b648ccd4818976879baba8772b3
Source noteuspto-grants-2008_05