HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(2-Chlorocyclohex-2-en-1-yl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | HCID 12211415 | HCID 12211415 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Chlorocyclohex-2-en-1-yl)-1H-isoindole-1,3(2H)-dione | HCID 14423979 | 73.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973585 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-7adae9eb705c475c82e314356ec2d4e6 |
| Source note | uspto-grants-1990_11 |