HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-2-methylpropanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(1-hydroxy-2-methylpropan-2-yl)-2,3-dihydro-1H-isoindole-1,3-dione | HCID 827789 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-2-methylpropanal | HCID 14578677 | 90.6% |
Reaction Steps
11.9 g of sulfur trioxide pyridine complex dissolved in 75 ml DMSO was added over a period of 20 minutes at room temperature to a solution of 5.48 g of 2-(2-hydroxy-1,1-dimethyl-ethyl)-isoindole-1,3-dione from Step 1 and 7.59 g of triethylamine in 780 ml DMSO. The reaction mixture was stirred at room temperature for 30 minutes, poured onto ice/water and extracted 3 times with tert-butyl methyl ether. The organic was washed with 1N HCl and 2 times H2O, dried over magnesium sulfate and the solvent was evaporated under reduced pressure to give 4.92 g crystals (mp 80-82° C.), which were used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507509B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a1080f6fd1964612b607db3a6bf5ca16 |
| Source note | uspto-grants-2013_08 |