Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 5-Bromo-7-chloro-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one | HCID 11704475 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 66873196 | HCID 66873196 | 44% |
Reaction Steps
A mixture of 5-bromo-7-chloro-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.781, 1.86 mmol), Pd(PPh3)4 (0.635 g, 0.55 mmol), KCN (0.357 g, 5.5 mmol), and KI (0.77 g, 4.65 mmol) in HMPA (8 mL) was stirred at 80° C. for 18 h. Workup and silica gel column chromatography using 2:1 hexanes-ethyl acetate (typically 2:1 hexane -EtOAc) afforded 3-Oxo-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-1H-isoindole-4,6-dicarbonitrile (0.300 g, 44%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.41 (s, 2H), 4.83 (s, 2H), 7.22 (d, 2H), 7.39 (d, 2H), 7.92 (s, 1H), 8.08 (s, 1H) GC-MS: m/z 357 (M)+, 272 (M-85)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968570B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-5f43986f1bf6447a9a7a1043665625a3 |
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| Source note | uspto-grants-2011_06 |
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