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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5063Generated: October 30, 2026

Dimethylformamide → HCID 131718111, compound

https://huagongshe.com/reaction/5063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(Iodomethyl)-5-methyl-2H-1,3-dioxol-2-oneHCID 18942137—
ReactantHCID 131718112HCID 131718112—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 131718111HCID 13171811145.7%

Reaction Steps

A solution of 66 mg of 5-methyl-2-oxo-1,3-dioxolen-4-ylmethyl iodide (prepared by heating 5-methyl-2-oxo-1,3-dioxolen-4-ylmethyl bromide and sodium iodide under reflux in acetone) in chloroform was added to a mixture of 47.6 mg of sodium (1R, 5S, 6S)-2-(2-oxo-3-pyrrolidinylthio)-6-[(1R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate and 0.4 ml of dry dimethylformamide. The mixture was stirred at room temperature for 80 minutes and then at 30°-45° C. for 4.5 hours. At the end of this time, the reaction mixture was diluted with ethyl acetate and washed four times with an aqueous solution of sodium chloride. The extract was dried and the solvent was distilled off under reduced pressure. The residue was purified by Lobar column chromatography (Merck, LiChroprep Si60, size A), eluted with a 10:1 by volume mixture of ethyl acetate and methanol, to give 27.4 mg of the title compound in the form of a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242914
Source datasetuspto-grants-1993_09
ORD IDord-d17197b3300b4c588249b50f58b34560
Source noteuspto-grants-1993_09