HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → 2-(3,3,3-Trifluoro-2-hydroxy-2-methylpropyl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86657675 | HCID 86657675 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(3,3,3-Trifluoro-2-hydroxy-2-methylpropyl)-1H-isoindole-1,3(2H)-dione | HCID 67383644 | — |
Reaction Steps
A mixture comprising 3,3,3-trifluoro-2-hydroxy-2-methyl-propyl-ammonium (0.9 g), phthalic anhydride (1.039 g) and DIPEA (2.188 ml) in chloroform (30 ml) was heated at 70° C. for 5 hours. After cooling to RT, the mixture was washed with water and passed through a phase separator. The organic phase was reduced to dryness. The crude product was purified by chromatography on silica, eluting in a 0% to 30% iso-hexane:EtOAc removed to give the title product; 1H NMR (400 MHz, Methanol-d4) δ 7.92 (2H, m), 7.85 (2H, m), 3.95 (2H, m), 1.36 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247436B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-246e82207b9d4c9fb802787ad100ca29 |
| Source note | uspto-grants-2012_08 |