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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120924Generated: November 1, 2026

Phthalimide → HCID 178425519, compound

https://huagongshe.com/reaction/2120924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
Reactant2,4,6-TrimethylanilineHCID 6913—
ReactantFerrous ChlorideHCID 24458—
SolventEthyl AcetateHCID 8857—
ProductHCID 178425519HCID 178425519—

Reaction Steps

A 100-mL round-bottom flask equipped with a nitrogen inlet and an internal fritted-glass filter is charged with phthalimide (2.94 g, 20.0 mmol) and ethyl acetate (60 mL). (The fritted-glass filter is attached to the end of a glass tube, which is inserted into the reactor through a rubber septum. The filter is easily raised above or lowered below the surface of liquids in the reactor.) 2,4,6-Trimethylaniline (5.41 g, 40.0 mmol, 2.0 eq.) and iron(II) chloride (2.54 g, 20.0 mmol) are added to the flask, and the mixture is stirred under nitrogen at room temperature for 1 h. The yellow mixture is heated to reflux (77° C.) for 10 h, and is then stirred at room temperature for 32 h. A brown precipitate forms. The reaction mixture is concentrated by stripping out the ethyl acetate under a stream of nitrogen. Cold diethyl ether (30 mL) is added to the residue, and the mixture is stirred to wash the residue. The glass filter is immersed in the liquid phase, which is then removed at reduced pressure through the internal filter. The solids are dried under vacuum for 2 h to give a brown powder. Yield: 10.11 g (99.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693154B2
Source datasetuspto-grants-2004_02
ORD IDord-f2fd48625b604e25a09bb6d56c2e5548
Source noteuspto-grants-2004_02