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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349300Generated: October 26, 2026

Dimethyl Sulfoxide → 7-(2-Formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl ester

https://huagongshe.com/reaction/349300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactantpyridine TFAHCID 9813011—
Reactant7-(2-Hydroxymethyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl esterHCID 69023030—
SolventBenzeneHCID 241—
Product7-(2-Formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl esterHCID 85973148—

Reaction Conditions

Temperature0 °C

Reaction Steps

EDCI (212 mg, 1.10 mmol) and DMSO (0.10 mL, 1.48 mmol) were added sequentially to a solution of 7-(2-hydroxymethyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl ester (100 mg, 0.37 mmol) in benzene (4.0 mL) at rt. The mixture was cooled to 0° C. and pyridinium trifluoroacetate (79 mg, 0.41 mmol) was added. The reaction was allowed to warm to rt and then was stirred at rt for 3.5 h. The solution was decanted from the oily residue and the residue was washed with benzene (3×3 mL). The combined benzene phases were concentrated in vacuo to afford crude 7-(2-formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl ester that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179820B2
Source datasetuspto-grants-2007_02
ORD IDord-c7f5f42b4fa44474887477c746409448
Source noteuspto-grants-2007_02