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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074145Generated: October 31, 2026

Diethyl Ether → 2-(2-Chlorocyclohex-2-en-1-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1074145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium IodideHCID 4875—
ReactantHCID 12211415HCID 12211415—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
Product2-(2-Chlorocyclohex-2-en-1-yl)-1H-isoindole-1,3(2H)-dioneHCID 1442397973.5%

Reaction Steps

A solution of 11.0 g (72.8 mmol) 1,6-dichlorocyclohexene, 20.0 g (108 mmol) potassium phthalimide and 1.0 g (6.0 mmol) potassium iodide in 50 ml dry dimethylformamide was stirred 24 hours at 110° C. under an atmosphere of nitrogen. The reaction mixture was allowed to cool then poured into 30 ml diethyl ether. The dark mixture was filtered then ether and DMF removed in vacuo. The dark crystalline residue was dissolved in ethyl acetate then chromatographed on 500 g flash silica eluting with 10% to 20% ethyl acetate/hexane. Concentration of appropriate fractions followed by recrystallization from ethyl acetate/hexane gave 14.0 g (73.5%) of the desired phthalimide, mp 99°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973585
Source datasetuspto-grants-1990_11
ORD IDord-7adae9eb705c475c82e314356ec2d4e6
Source noteuspto-grants-1990_11