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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361166Generated: October 31, 2026

5-Methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amide → 1-(5-Methanesulfonyl-furan-2-yl)-propan-1-one

https://huagongshe.com/reaction/1361166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amideHCID 59278485—
ReactantHCID 178461633HCID 178461633—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Methanesulfonyl-furan-2-yl)-propan-1-oneHCID 59278141—

Reaction Steps

To a chilled (0° C.) solution of 5-methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amide (1.48 g, 6.36 mmol) in THF (30 mL) was added a 2 M solution of ethylmagnesium chloride in THF (7.0 mL, 14 mmol). The mixture was then slowly warmed to with stirring. After 18 hours, the mixture was quenched with saturated aqueous ammonium chloride (50 mL) and then diluted with ethyl acetate (50 mL). The aqueous phase was separated and extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated to afford 1-(5-methanesulfonyl-furan-2-yl)-propan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-6ea0f09aa53845f0bea7afba976b5c29
Source noteuspto-grants-2011_02