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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052926Generated: October 27, 2026

Dimethyl Sulfoxide → 7-((R)-2-formyl-6-oxo-piperidin-1-yl)-hept-5-enoic acid methyl ester

https://huagongshe.com/reaction/2052926

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)-hept-5-enoic acid methyl esterHCID 69022896—
SolventBenzeneHCID 241—
Product7-((R)-2-formyl-6-oxo-piperidin-1-yl)-hept-5-enoic acid methyl esterHCID 86595296—

Reaction Conditions

Temperature0 °C

Reaction Steps

EDCI (36 mg, 0.19 mmol) and DMSO (18 μL, 0.25 mmol) were added sequentially to a solution of 7-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-hept-5-enoic acid methyl ester (16.7 mg, 0.062 mmol) in benzene (1.0 mL) at rt. The mixture was cooled to 0° C. and pyridinium trifluoroacetate (13.2 mg, 0.068 mmol) was added. The reaction was allowed to warm to rt and then was stirred at rt for 2.5 h. The solution was decanted from the oily residue and the residue was washed with benzene (3×1 mL). The combined benzene phases were concentrated in vacuo to afford crude 7-((R)-2-formyl-6-oxo-piperidin-1-yl)-hept-5-enoic 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-c0ab961e586b4b82bdd077d825947c05
Source noteuspto-grants-2008_02