Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 58914719 | HCID 58914719 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10288570 | HCID 10288570 | 32% |
Reaction Steps
Combine 3,3-Bis-[4-(tert-butyl-dimethyl-silanyloxy)-3,5-dimethyl-phenyl]-1,3-dihydro-indol-2-one (0.886 g, 1.47 mmol), p-tolylboronic acid (0.40 g, 2.94 mmol), copper (II) acetate (0.267 g, 1.47 mmol), triethylamine (0.41 mL, 2.94 mmol), 4 angstrom molecular sieves, and dichloromethane (20 mL). Stir at room temperature overnight under ambient atmosphere. Filter the reaction through Celite. Elute through a column of silica gel with 70% dichloromethane in hexanes and concentrate. Dissolve the resulting compound (0.340 g, 0.492 mmol), in THF (2 mL). Add a solution of tetrabutylammonium fluoride (1.0 M) in THF (1.23 mL). Stir for 1 h. Add 1N aqueous HCl(10 mL), water (40 mL), and ethyl acetate (50 mL). Separate the layers and concentrate the organic layer in vacuo. Chromatograph on silica gel eluting with ethyl acetate to give 0.215 g (32%) of the title compound: mass spectrum (FAB): m/z=464(M+1); 1H NMR(DMSO-d6): δ8.23 (s, 2H), 7.37-7.28 (m, 5H), 7.21 (td, 1H), 7.08 (td, 1H), 6.74-6.73 (m, 5H), 2.37 (s, 3H) 2.07 (s, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250442B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-aed7d47a8440446b8c8e08bc2b61a089 |
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| Source note | uspto-grants-2007_07 |
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