Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | HCID 67185185 | HCID 67185185 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67187623 | HCID 67187623 | 13.4% |
Reaction Steps
To a solution of Example 441 (100 mg, 0.2 mmol) in EtOH (4 mL) was added cyclohexene (1 mL) and palladium on carbon (120 mg, 10% wt). The reaction mixture was heated at 120° C. under microwave irradiation for 1 h. Additional palladium on carbon (40 mg, 10% wt) was added and the reaction mixture heated at 130° C. under microwave irradiation for 5 h. The reaction mixture was filtered through celite and concentrated in vacuo. Purification by preparative HPLC (Method 6) gave the title compound (12.5 mg, 12.5%) as a brown solid. δH (CDCl3) 8.11 (1H, d, J 2.4 Hz), 7.42 (1H, dd, J 8.1 and 7.3 Hz), 7.01 (1H, dd, J 8.9 and 2.4 Hz), 6.92 (1H, d, J 8.7 Hz), 6.68 (1H, d, J 7.9 Hz), 6.64 (1H, d, J 7.3 Hz), 6.42 (1H, br. s), 5.15 (1H, br. s), 4.26-4.38 (2H, m), 4.18-4.08 (2H, m), 3.76 (2H, t, J 6.8 Hz), 3.36 (3H, s), 2.94 (2H, t, J 6.8 Hz), 2.87 (2H, s), 1.39 (6H, s). LCMS (ES+) 466.18 (M+H)+, RT 2.17 minutes (Method 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242116B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-29bf043dc19e4225ae17ad1b9e3994e8 |
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| Source note | uspto-grants-2012_08 |
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