Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 58906751 | HCID 58906751 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 69069452 | HCID 69069452 | — |
Reaction Steps
To a solution of 4-(5-Cyclopropyl-pent-3-ynyl)-2,2-dimethyl-[1,3]dioxolane (1.92 mmol, 0.40 g) in hexane (5 mL) was added quinoline (0.192 mmol, 24.8 mg), followed by addition of 5% Pd on BaSO4 (0.384 mmol). Stirred at room temperature under H2 atmosphere for 4 hrs. TLC showed reaction completed. Filtered through celite and concentrated. Diluted with hexane, washed with NH4Cl, brine and dried over MgSO4. Silica gel chromatography (2˜7% EtOAc/Hexane) 4-(5-Cyclopropyl-pent-3-enyl)-2,2-dimethyl-[1,3]dioxolane as clear oil 1H NMR (400 MHz, CDCl3): δ 5.52–5.45 (m, 1H), 5.40–5.34 (m, 1H), 4.11–4.04 (m, 1H), 4.02 (dd, 1H, J1=8.0 Hz, J2=6.0 Hz), 3.51 (t, 1H, J=7.5 Hz), 2.17–2.04 (m, 2H), 1.97 (t, 2H, J=7.0 Hz), 1.74–1.66 (m, 1H), 1.58–1.49 (m, 1H), 1.41 (s, 3H), 1.35 (s, 3H), 0.73–0.68 (m, 1H), 0.43–0.39 (m, 2H), 0.08–0.04 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241792B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-9f7d73de2cd7439589d6b8e6abc4b217 |
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| Source note | uspto-grants-2007_07 |
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