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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052914Generated: October 26, 2026

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

https://huagongshe.com/reaction/2052914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactantpyridine TFAHCID 9813011—
Reactant7-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl esterHCID 69023025—
SolventBenzeneHCID 241—
Product7-((R)-2-formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl esterHCID 86595294—

Reaction Conditions

Temperature0 °C

Reaction Steps

EDCI (119 mg, 0.62 mmol) and DMSO (59 μL, 0.83 mmol) were added sequentially to a solution of 7-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl ester (56 mg, 0.21 mmol) in benzene (2.0 mL) at rt. The mixture was cooled to 0° C. and pyridinium trifluoroacetate (44 mg, 0.23 mmol) was added. The reaction was allowed to warm to rt and then was stirred at rt for 3 h. The solution was decanted from the oily residue and the residue was washed with benzene (3×2 mL). The combined benzene phases were concentrated in vacuo to afford crude 7-((R)-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 numberUS07326716B2
Source datasetuspto-grants-2008_02
ORD IDord-d9d0aefd955c452495ef736ce7339099
Source noteuspto-grants-2008_02