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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066390Generated: October 26, 2026

3-Hydroxyacetophenone → 3-(2-Hydroxypropan-2-yl)phenol

https://huagongshe.com/reaction/2066390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Hydroxypropan-2-yl)phenolHCID 458142—

Reaction Steps

3′-Hydroxyacetophenone (500 mg) was dissolved in tetrahydrofuran (10 ml), and the solution was slowly added dropwise with a 3 M solution of methylmagnesium bromide in diethyl ether (3.7 ml) under ice cooling. The mixture was stirred at the same temperature for 2 hours, and then added with saturated aqueous ammonium chloride, the mixture was extracted with ethyl acetate, and the organic layer was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1 to 1:1) to obtain the title compound (224.3 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293715B2
Source datasetuspto-grants-2012_10
ORD IDord-39c07a8b5ee34016b3b834139786b5f3
Source noteuspto-grants-2012_10