Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 54703388 | HCID 54703388 | — |
| Catalyst | Pd barium sulfate | HCID 16218511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54684903 | HCID 54684903 | — |
Reaction Steps
Quinoline (70 μL, 0.6 mmol), 15 mg of 5% Pd/BaSO4 and 61 mg (0.25 mmol) of 3,4-dihydroxy-5-[(4-phenyl)-3-butynyl]-2(5H)-furanone were combined in 20 mL of ethanol and hydrogenated at atmospheric pressure until 12 mL (0.5 mmol) of H2 was consumed as measured by a H2O filled burette. The catalyst was removed by filtration through two #1 fluted filter papers and the solution was concentrated to a volume of about 5 mL, taken up in SOmL of ether and washed with 3×15 mL of 5% aqueous HCl, 20 mL of H2O and 20 mL of brine, dried (MgSO4) and concentrated to provide 3,4-dihydroxy-5-(4-phenylbutanyl)-2(5H)-furanone as a brown wax: 1H NMR (acetone-d6) δ 7.28-7.13 (m, 5H), 4.66 (dd, J=3.4, 7.2 Hz, 1H), 2.62 (t, J=7.7, 2H), 2.00-1.93 (m, 1H), 1.69-1.42 (m, 5H); 13C NMR (acetone-d6) δ 170.7, 154.9, 143.3, 129.2, 129.1, 126.5, 118.6, 76.2, 36.3, 32.7, 32.1, 24.6. Anal Calcd for C14H16O4 +0.25 H2O: C, 66.52; H, 6.58. Found: C, 66.71; H, 6.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136832 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-cd420eb1c26540b0ba0bbbb8f4306a9b |
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| Source note | uspto-grants-2000_10 |
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