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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243545Generated: October 29, 2026

Triethylamine → 3-(4,5,6,7-Tetrafluoro-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedione

https://huagongshe.com/reaction/1243545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
ReactantHCID 21928258HCID 21928258—
SolventDimethylformamideHCID 6228—
Product3-(4,5,6,7-Tetrafluoro-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedioneHCID 12972138—

Reaction Steps

A mixture of 16.25 g of 2,6-dioxopiperidin-3-ammonium chloride, and 30.1 g of methyl 2-bromomethyl-3,4,5,6-tetrafluorobenzoate, and 12.5 g of triethylamine in 100 mL of dimethylformamide is stirred at room temperature for 15 hours. The mixture is then concentrated in vacuo and the residue mixed with methylene chloride and water. The aqueous layer is separated and back-extracted with methylene chloride. The combined methylene chloride solutions are dried over magnesium sulfate and concentrated in vacuo to give 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119106B2
Source datasetuspto-grants-2006_10
ORD IDord-40548e0452734cfa84c634f269ad9a1f
Source noteuspto-grants-2006_10