HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[3-(2,2-Dimethyl[1,3]dioxolan-4-yl)propyl]isoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(2,2-Dimethyl-1,3-dioxolan-4-yl)propan-1-amine | HCID 13416686 | — |
| Reactant | Ethoxycarbonylphthalimide | HCID 22254400 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[3-(2,2-Dimethyl[1,3]dioxolan-4-yl)propyl]isoindole-1,3-dione | HCID 21915469 | — |
Reaction Steps
To a stirred solution of 3-(2,2-dimethyl-[1,3]dioxolan-4-yl)propylamine (1.05 g, 6.60 mmol) and carboethoxyphthalimide (1.45 g, 6.60 mmol) in acetonitrile (10 mL) at room temperature was added triethylamine (0.92 mL, 6.60 mmol) in one portion and the resuting mixture was stirred at room temperature for 18 hours, evaporated in vacuo and the residue was dissolved in ethyl acetate (50 mL). The solution was washed with brine, 10% citric acid solution and brine, then dried over anhydrous magnesium sulfate. Filtration and concentration in vacuo gave an oil which was purified by column chromatography on silica using ethyl acetate—petroleum ether mixture as eluent to afford a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259271B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-600ec312e58a451ca0ee3f0d599d4ced |
| Source note | uspto-grants-2007_08 |