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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064108Generated: November 1, 2026

Triethylamine → 1-Oxo-2-(2,6-dioxopiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline

https://huagongshe.com/reaction/2064108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
ReactantHCID 21928258HCID 21928258—
SolventDimethylformamideHCID 6228—
Product1-Oxo-2-(2,6-dioxopiperidin-3-yl)-4,5,6,7-tetrafluoroisoindolineHCID 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 numberUS08288415B2
Source datasetuspto-grants-2012_10
ORD IDord-cd7491cd96184288906911aa21729c30
Source noteuspto-grants-2012_10