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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198137Generated: October 30, 2026

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

https://huagongshe.com/reaction/2198137

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 stifling. 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 numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-71eb9509db35408fbd3d650311bc797b
Source noteuspto-grants-2012_12