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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066392Generated: November 2, 2026

3-Hydroxyacetophenone → HCID 67387533, compound

https://huagongshe.com/reaction/2066392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67387533HCID 67387533—

Reaction Steps

3′-Hydroxyacetophenone (5.0 g) was dissolved in tetrahydrofuran (100 ml), and the solution was added dropwise with a 1 M solution of phenylmagnesium bromide in tetrahydrofuran (100 ml) at −30° C. Then mixture was further added with tetrahydrofuran (100 ml), and the mixture was stirred for 3 hours with gradually warming it. The mixture was added with saturated aqueous ammonium chloride under ice cooling, 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=2:1 to 1:1) to obtain the title compound (7.55 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293715B2
Source datasetuspto-grants-2012_10
ORD IDord-f0db1c6c5ced43d1aef3cb5376bac90a
Source noteuspto-grants-2012_10