Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734475Generated: October 25, 2026

Tetrahydrofuran → 1-(3-Methoxy-2-methylphenyl)ethanone

https://huagongshe.com/reaction/734475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Methoxy-2-MethylBenzoic AcidHCID 7021483—
ReactantHCID 178418573HCID 178418573—
CatalystIron (III) acetylacetonateHCID 11110968—
SolventThionyl ChlorideHCID 24386—
Product1-(3-Methoxy-2-methylphenyl)ethanoneHCID 19702342—

Reaction Steps

A solution of 2-methyl-3-methoxybenzoic acid (10.0 g, 60.2 mmol) in thionyl chloride (50 ml) was heated at reflux for 1 h and then cooled and concentrated in vacuo. To the residue was added tetrahydrofuran (100 ml) and iron (III) acetylacetonate (638 mg, 1.8 mmol) and the solution was cooled to −20° C., before addition of methylmagnesium bromide (3M in diethyl ether, 22.1 ml, 66.2 mmol). After stirring for 15 min, the mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane. The combined extracts were washed with saturated aqueous sodium hydrogen carbonate solution, dried (MgSO4) and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592362B2
Source datasetuspto-grants-2009_09
ORD IDord-99abc8a9768d498693285ed446c76140
Source noteuspto-grants-2009_09